Электронная библиотечная система КОНСУЛЬТАНТ СТУДЕНТА
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wrap-content-read table-responsive">ap-content-read table-responsive">-content-read table-responsive">tent-read table-responsive">nt-read table-responsive">-read table-responsive">asss=-stickertickercker5-0031-00010031-000131-0001-00010011"2>) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.ofacial dysmorphia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.acial dysmorphia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.ial dysmorphia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.dysmorphia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.smorphia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.phia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.ia) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.) are not uncommon. According to etiology, they may be hereditary, multifactorial and intrauterine.e hereditary, multifactorial and intrauterine.hereditary, multifactorial and intrauterine.reditary, multifactorial and intrauterine.tary, multifactorial and intrauterine.ry, multifactorial and intrauterine., multifactorial and intrauterine.>, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.rphological manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.hological manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.logical manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.gical manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.cal manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.l manifestations, these malformations are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.ns are divided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.vided into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.ded into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.d into developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.to developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands. developmental abnormalities of the face, jaws and lips, teeth, their enamel and dentin, tongue, salivary glands.livary glands.ivary glands., in which ducts of small salivary glands open); Fordyce granules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts). in some cases they are concealed: subcutaneous or submucosal.n some cases they are concealed: subcutaneous or submucosal.some cases they are concealed: subcutaneous or submucosal.me cases they are concealed: subcutaneous or submucosal.ses they are concealed: subcutaneous or submucosal.s they are concealed: subcutaneous or submucosal.they are concealed: subcutaneous or submucosal.lassssper lip in the projection of the upper lateral incisor tooth (hare lip, cheiloschisis) and cleft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.r lip in the projection of the upper lateral incisor tooth (hare lip, cheiloschisis) and cleft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.lip in the projection of the upper lateral incisor tooth (hare lip, cheiloschisis) and cleft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.p in the projection of the upper lateral incisor tooth (hare lip, cheiloschisis) and cleft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.in the projection of the upper lateral incisor tooth (hare lip, cheiloschisis) and cleft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ft palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. palate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ate (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.e (palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.(palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.b>(palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.(palatoschisis) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.s) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome./i>) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.>) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome./b>) account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. account for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ccount for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. for up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.or up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. up to 45% of all orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ll orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. orofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.rofacial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.acial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ial malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.l malformations, and in half of cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.f cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.cases, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ses, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.s, they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. they are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.hey are combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.re combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. combined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ombined - cheilopalatoschisis (fig. 27.1), and in 15% are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. are associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.re associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. associated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.iated with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ted with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.d with other defects. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.cts. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.s. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. Often, a retained or absent maxillary lateral incisor is noted. The combination of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ion of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.n of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.of palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. palatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.alatoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.atoschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.oschisis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.isis with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.is with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. with small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.h small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.small size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.size of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ze of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. of the lower jaw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.aw bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. bone (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.one (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome. (lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.>lower micrognathia) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.) and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.and tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.d tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.tongue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ngue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.ue (microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.b>microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.>microglossia) with tongue retraction (glossoptosis) and impaired breathing is called Pierre Robin s­yndrome.i>) and impaired breathing is called Pierre Robin s­yndrome.) and impaired breathing is called Pierre Robin s­yndrome.b>) and impaired breathing is called Pierre Robin s­yndrome.d impaired breathing is called Pierre Robin s­yndrome.impaired breathing is called Pierre Robin s­yndrome.paired breathing is called Pierre Robin s­yndrome.is called Pierre Robin s­yndrome. called Pierre Robin s­yndrome.alled Pierre Robin s­yndrome.t">When the palatal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.en the palatal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children. the palatal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.he palatal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.alatal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.atal cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.al cleft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.left is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ft is cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.cross-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.oss-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.s-cutting, newborns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.orns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ns have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children. have breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ve breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children. breathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.reathing, sucking and swallowing disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ng disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children. disorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.isorders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.orders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ders, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.rs, which leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.hich leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.ch leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children. leads to ingress of food masses from the mouth into the nasopharynx and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.x and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.and their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.d their aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.r aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.aspiration with the development of aspiration pneumonia. With age, speech disorders develop in such children.piration with the development of aspiration pneumonia. With age, speech disorders develop in such children. development of aspiration pneumonia. With age, speech disorders develop in such children.evelopment of aspiration pneumonia. With age, speech disorders develop in such children.elopment of aspiration pneumonia. With age, speech disorders develop in such children.xtb>Fordyce granules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.rdyce granules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.yce granules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.e granules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.anules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ules (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.b> (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. (Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.Fordyce disease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.isease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ease, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.se, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases./i>, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.>, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases./b>, Fox-Fordyce disease, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases., seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.i>, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases., seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.b>, seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases., seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.>seborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.eborrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.orrheic cysts) are clusters of enlarged sebaceous glands without excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.thout excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.out excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.t excretory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.etory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ory ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.y ducts or with impaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.mpaired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.aired patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.red patency in the form of nodules 1-2 mm in size and yellowish in color on the lips and mucous membrane of the cheeks, esophagus, as well as in the area of genital organs, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ans, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.s, breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. breast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.reast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ast nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.t nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.nipples. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.les. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.s. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. 35% of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. of patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.f patients with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ents with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ts with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. with Fordyce granules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.ranules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.nules are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.les are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. are women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases.re women and 60% are men. Such formations are regarded as a variant of the norm; however, they cause cosmetic defects, and can also be mistaken for tumors or skin diseases. women and 60% are men. 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dotted #c0c0c0;cursor:hand;">c0;cursor:hand;">;cursor:hand;">ursor:hand;">sor:hand;">r:hand;">hand;">nd;">>Fig. 27.1. Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis)Fig. 27.1. Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis)g. 27.1. Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis)27.1. Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis).1. Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis). Lateral left-sided cleft of the upper lip, alveolar process, and hard palate (cheilopalatoschisis) of the upper lip, alveolar process, and hard palate (cheilopalatoschisis)f the upper lip, alveolar process, and hard palate (cheilopalatoschisis)the upper lip, alveolar process, and hard palate (cheilopalatoschisis)e upper lip, alveolar process, and hard palate (cheilopalatoschisis)upper lip, alveolar process, and hard palate (cheilopalatoschisis)per lip, alveolar process, and hard palate (cheilopalatoschisis)ip, alveolar process, and hard palate (cheilopalatoschisis), alveolar process, and hard palate (cheilopalatoschisis)alveolar process, and hard palate (cheilopalatoschisis)lassxt malformation is alcohol syndrome (alcoholic embryofetopathy) in children born by women who systematically consumed alcohol during pregnancy: hypognathism, in 7% - high hard palate, cleft upper lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.alformation is alcohol syndrome (alcoholic embryofetopathy) in children born by women who systematically consumed alcohol during pregnancy: hypognathism, in 7% - high hard palate, cleft upper lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.formation is alcohol syndrome (alcoholic embryofetopathy) in children born by women who systematically consumed alcohol during pregnancy: hypognathism, in 7% - high hard palate, cleft upper lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.t upper lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.upper lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.per lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.r lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.lip and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.p and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.and palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.palate (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.late (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.te (cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.cheilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.eilopalatoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.latoschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.toschisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.schisis), malformations of the nervous, cardiovascular, genitourinary systems, extremities.rmations of the nervous, cardiovascular, genitourinary systems, extremities.ations of the nervous, cardiovascular, genitourinary systems, extremities.ions of the nervous, cardiovascular, genitourinary systems, extremities.s of the nervous, cardiovascular, genitourinary systems, extremities.of the nervous, cardiovascular, genitourinary systems, extremities. the nervous, cardiovascular, genitourinary systems, extremities.genitourinary systems, extremities.nitourinary systems, extremities.tourinary systems, extremities.urinary systems, extremities.inary systems, extremities.ary systems, extremities.ystems, extremities.tems, extremities.ms, extremities.f teeth, their enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth, their enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eth, their enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.heir enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ir enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. enamel and dentin are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.n are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss./b> are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.> are extremely diverse. These include the following disorders: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ers: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.s: number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.i>number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.number of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.mber of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.er of teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.f teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eth (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss./i> (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.> (edentia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ntia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ia, hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss., hypodontia or oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. oligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ligodontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.godontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ontia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.tia, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.a, hyperodontia, dichotomy of teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eth); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.h); teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.; teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.>teeth location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.h location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.location (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.cation (retained and impacted teeth); size and shape of teeth (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.h (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss./i> (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.> (macrodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.rodontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.dontia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ntia, microdontia, reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss., reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.reduction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.duction or increase in the quantity of cusps, roots, their length, forms, fusion of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.on of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. of teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.f teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eth, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.h, etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. etc.); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss..); eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.; eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ruption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ption can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss./i> can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.> can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.can be premature (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.e (natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.(natal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.atal teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.l teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.teeth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.eth that are present at birth), or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss., or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.or delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. delayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.elayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ayed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.ed, for instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.or instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. instance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss.nstance, in congenital hypothyroidism, gingival fibromatosis, etc.; premature teeth loss. premature teeth loss.i>premature teeth loss.premature teeth loss.ure teeth loss.e teeth loss.teeth loss.pigmentation, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).gmentation, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).entation, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).tation, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).tion, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).on, imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”)., imperfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).perfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).rfect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).ect amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).amelogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).elogenesis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).esis, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).is, enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”)., enamel hypoplasia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).asia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).ia and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”). and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).> and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).and imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”).d imperfect dentinogenesis (see section “Non-carious lesions of dental tissue”)./i> (see section “Non-carious lesions of dental tissue”).> (see section “Non-carious lesions of dental tissue”).(see section “Non-carious lesions of dental tissue”).ee section “Non-carious lesions of dental tissue”). section “Non-carious lesions of dental tissue”).ection “Non-carious lesions of dental tissue”).n “Non-carious lesions of dental tissue”).“Non-carious lesions of dental tissue”).dquo;Non-carious lesions of dental tissue”).asss=t">rmations include: aglossia (congenital lack of tongue); micro- or hypoglossia (tongue underdevelopment); macroglossia (tongue enlargement), cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ations include: aglossia (congenital lack of tongue); micro- or hypoglossia (tongue underdevelopment); macroglossia (tongue enlargement), cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ions include: aglossia (congenital lack of tongue); micro- or hypoglossia (tongue underdevelopment); macroglossia (tongue enlargement), cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy). cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).i>cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).cleft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).eft tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).t tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).tongue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ngue; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).i>; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).; ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).>ankyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).nkyloglossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).lossia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ssia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ia (deformaty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).ty or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy). or misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).r misplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).isplaced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).placed attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).aced attachment of the tongue frenulum); lingual goiter (thyroid heterotopy).frenulum); lingual goiter (thyroid heterotopy).enulum); lingual goiter (thyroid heterotopy).ulum); lingual goiter (thyroid heterotopy).um); lingual goiter (thyroid heterotopy).); lingual goiter (thyroid heterotopy). lingual goiter (thyroid heterotopy).ingual goiter (thyroid heterotopy).gual goiter (thyroid heterotopy).al goiter (thyroid heterotopy).b>Malformations of salivary glands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.Malformations of salivary glands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.mations of salivary glands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.tions of salivary glands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.ons of salivary glands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.lands are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.nds are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.s are represented by aplasia and hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.d hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.>hypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.ypoplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.oplasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.lasia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.sia; atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis. atresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.tresia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.esia and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis. and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.i> and doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis. doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.i>doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.doubling of the ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis. ducts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); adenomatoid hyperplasia, polycystic parotid glands, as well as xerostomy (“dry syndrome”), which contributes to the development of caries and periodontitis.ucts of large salivary glands; ectopy of salivary glands (in the lymph nodes and soft tissues of the head and neck, jaw bones, tonsils); 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