hereditary motor & sensory neuropathy

A group of conditions dignified by eponym and subdivided as follows. hereditary motor & sensory neuropathy Type I Charcot-Marie-Tooth disease, hypertrophic form An AD–type 1a, type 1b, or X-linked condition that is the most common form of HMSN, characterized by a slowly progressive disease of childhood onset with predominantly motor symptoms, pes cavus, calf atrophy, very slow motor impulse conduction with segmental demyelination and remyelination with 'onion-bulb' formation Type II Roussy-Levy syndrome, or Charcot-Marie-Tooth disease, neuronal form An AD condition characterized by slowly progressive disease of adolescent onset with predominantly motor symptoms, clubfoot deformity, calf atrophy, mild reduction in impulse transmission and 'onion-bulb' formation Type III Dejerine-Sottas disease A rare relentlessly progressive AD condition of infant onset with short stature, scoliosis, pes cavus, calf atrophy, very slow conduction of motor impulses with segmental demyelination and remyelination 'onion-bulb' formation. See Hereditary sensory neuropathy.

hereditary motor & sensory neuropathy

单词	hereditary motor & sensory neuropathy
释义	hereditary motor & sensory neuropathy hereditary motor & sensory neuropathy A group of conditions dignified by eponym and subdivided as follows. hereditary motor & sensory neuropathy Type I Charcot-Marie-Tooth disease, hypertrophic form An AD–type 1a, type 1b, or X-linked condition that is the most common form of HMSN, characterized by a slowly progressive disease of childhood onset with predominantly motor symptoms, pes cavus, calf atrophy, very slow motor impulse conduction with segmental demyelination and remyelination with 'onion-bulb' formation Type II Roussy-Levy syndrome, or Charcot-Marie-Tooth disease, neuronal form An AD condition characterized by slowly progressive disease of adolescent onset with predominantly motor symptoms, clubfoot deformity, calf atrophy, mild reduction in impulse transmission and 'onion-bulb' formation Type III Dejerine-Sottas disease A rare relentlessly progressive AD condition of infant onset with short stature, scoliosis, pes cavus, calf atrophy, very slow conduction of motor impulses with segmental demyelination and remyelination 'onion-bulb' formation. See Hereditary sensory neuropathy. hereditary motor & sensory neuropathy hereditary motor & sensory neuropathy A group of conditions dignified by eponym and subdivided as follows. hereditary motor & sensory neuropathy Type I Charcot-Marie-Tooth disease, hypertrophic form An AD–type 1a, type 1b, or X-linked condition that is the most common form of HMSN, characterized by a slowly progressive disease of childhood onset with predominantly motor symptoms, pes cavus, calf atrophy, very slow motor impulse conduction with segmental demyelination and remyelination with 'onion-bulb' formation Type II Roussy-Levy syndrome, or Charcot-Marie-Tooth disease, neuronal form An AD condition characterized by slowly progressive disease of adolescent onset with predominantly motor symptoms, clubfoot deformity, calf atrophy, mild reduction in impulse transmission and 'onion-bulb' formation Type III Dejerine-Sottas disease A rare relentlessly progressive AD condition of infant onset with short stature, scoliosis, pes cavus, calf atrophy, very slow conduction of motor impulses with segmental demyelination and remyelination 'onion-bulb' formation. See Hereditary sensory neuropathy.
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