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Up to: Hereditary disease · Syndromic disease
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome
A rare demyelinating hereditary motor and sensory neuropathy characterized by early-onset, slowly progressive, distal muscular weakness and atrophy with no sensory impairment, congenital sensorineural deafness and mild intellectual disability (with absence of normal speech development). The absence of large myelinated fibers on sural nerve biopsy is equally characteristic of the disease.
This condition has no sub-types.