Other terms
Neuropathies, Hereditary Motor and Sensory,HMSN,Hereditary Motor and Sensory Neuropathies,Herditary Sensory and Motor Neuropathy,HMSN Type III,HMSN Type IIIs,Hereditary, Type III, Motor and Sensory Neuropathy,Dejerine-Sottas Disease,Dejerine Sottas Disease,Disease, Dejerine-Sottas,Hereditary, Type VII, Motor and Sensory Neuropathy,HMSN Type VII,HMSN Type VIIs,Type VII, HMSN
Description
Hereditary Sensory and Motor Neuropathy: 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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