En grupp långsamt fortskridande, ärftliga sjukdomar som drabbar perifera motoriska nerver och känselnerver, och som omfattar typerna HMSN I-VII. HMSN I och II avser Charcot-Marie-Tooths sjukdom. HMSN III avser hypertrofisk neuropati hos barn, HMSN IV är Refsums sjukdom, HMSN V avser ett tillstånd med ärftlig motorisk och sensorisk nervsjukdom i kombination med spastisk paraplegi. HMSN VI är förenad med synnervsatrofi och HMSN VII är förenad med retinitis pigmentosa.
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)
Dejerine-Sottas sjukdom — Charcot-Marie-Tooths sjukdom typ 3 — Ärftlig sensorisk och motorisk neuropati — Dejerine-Sottas neuropati — Hereditär motorisk och sensorisk neuropati, typ VII
Neuropathies, Hereditary Motor and Sensory — Hereditary Motor and Sensory Neuropathy — HMSN — Herditary Sensory and Motor Neuropathy — Hereditary Motor and Sensory Neuropathies — Hereditary, Type VII, Motor and Sensory Neuropathy — HMSN Type VII — HMSN Type VIIs — Type VII, HMSN — HMSN Type III — HMSN Type IIIs — Charcot-Marie-Tooth Disease, Type 3 — Charcot Marie Tooth Disease, Type 3 — CMT4f — Dejerine-Sottas Disease — Dejerine Sottas Disease — Disease, Dejerine-Sottas — Dejerine-Sottas Neuropathy — Dejerine Sottas Neuropathy — Neuropathy, Dejerine-Sottas — Hereditary, Type III, Motor and Sensory Neuropathy — HMSN3 — Hereditary Motor and Sensory Neuropathy 3 — Hypertrophic Neuropathy of Dejerine-Sottas — Dejerine-Sottas Hypertrophic Neuropathy — Hypertrophic Neuropathy of Dejerine Sottas — Hereditary Motor and Sensory Neuropathy Type III — Charcot-Marie-Tooth Disease, Demyelinating, Type 4f — Dejerine-Sottas Syndrome — Dejerine Sottas Syndrome — Syndrome, Dejerine-Sottas