Déjerineov-Sottasov syndróm Déjerineova-Sottasova choroba neuropatie dedičné motorické a senzorické neuropatia dedičná motorická a senzorická, typ VII neuropatia dedičná motorická a senzorická, typ III HMSN HMSN, typ III HMSN, typ VII
English X references
Dejerine-Sottas Disease HMSN HMSN Type III HMSN Type VII Hereditary Motor and Sensory Neuropathies Hereditary, Type III, Motor and Sensory Neuropathy Hereditary, Type VII, Motor and Sensory Neuropathy Neuropathies, Hereditary Motor and Sensory
Scope note in English
A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)
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