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
Herditary Sensory and Motor Neuropathy — Hereditary Motor and Sensory Neuropathies — Hereditary Motor and Sensory Neuropathy — HMSN — Neuropathies, Hereditary Motor and Sensory — HMSN Type III — HMSN Type IIIs — Charcot-Marie-Tooth Disease, Demyelinating, Type 4f — 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 — Dejerine-Sottas Syndrome — Dejerine Sottas Syndrome — Syndrome, Dejerine-Sottas — Hereditary Motor and Sensory Neuropathy 3 — Hereditary Motor and Sensory Neuropathy Type III — Hereditary, Type III, Motor and Sensory Neuropathy — HMSN3 — Hypertrophic Neuropathy of Dejerine-Sottas — Dejerine-Sottas Hypertrophic Neuropathy — Hypertrophic Neuropathy of Dejerine Sottas — HMN (Hereditary Motor Neuropathy) Proximal Type I — Proximal Hereditary Motor Neuropathy Type I — Hereditary, Type VII, Motor and Sensory Neuropathy — HMSN Type VII — HMSN Type VIIs — Type VII, HMSN