Chapter 17. Neuromuscular diseases

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17.3. Hereditary motor-sensory neuropathies types I and II

17.3.1. Hereditary Motor Sensory Neuropathies Type I

17.3.2. Hereditary Motor Sensory Neuropathies Type II

17.4. Paroxysmal myoplegia

17.4.1. Hypokalemic Form of Paroxysmal Myoplegia (Westphal’s Disease)

17.4.2. Hyperkalemic Form of Paroxysmal Myoplegia (Gamstorp Disease)

17.4.3. Normokalemic (Periodic) Paralysis

17.5. Myotonia

17.5.1. Congenital Myotonia (Leiden-Thomsen-Becker Disease)

17.5.2. Rossolimo-Curschmann-Batten-Steinert Myotonic Dystrophy

Chapter 18. Myasthenia Gravis

Chapter 19. Motor Neuron Disease

Chapter 20. Malformations of the Nervous System +

Chapter 21. Dementia +

Chapter 22. Pain

Chapter 23. Autonomic Nervous System Disorders +

Chapter 24. Headache +

Chapter 25. Neurotic disorders +

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Chapter 12. Demyelinating Diseases +

Chapter 13. Epilepsy +

Chapter 14. Diseases of the Peripheral Nervous System +

Chapter 15. Neurological Complications of Degenerative Disc Disease

Chapter 16. Degenerative Diseases of the Nervous System +

Chapter 17. Neuromuscular diseases -

17.1. Progressive muscular dystrophy

17.1.1. Duchenne Progressive Muscular Dystrophy

17.1.2. Emery–Dreifuss Progressive Muscular Dystrophy

17.1.3. Limb-Girdle Forms of Progressive Muscular Dystrophy

17.1.4. Landouzy-Dejerine Facioscapulohumeral Muscular Dystrophy

17.2. Spinal amyotrophy

17.2.1. Werdnig-Hoffmann Spinal Amyotrophy (Type I)

17.2.2. Chronic Infantile Spinal Amyotrophy (Type II)

17.2.3. Kugelberg–Welander Spinal Amyotrophy (Type III)