Charcot-Marie-Tooth disease type 1

Charcot-Marie-Tooth disease type 1 (CMT1) is a group of autosomal dominant demyelinating peripheral neuropathies characterized by distal weakness and atrophy, sensory loss, foot deformities, and slow nerve conduction velocity.

Also known as: CMT1, Charcot-Marie-Tooth neuropathy type 1, autosomal dominant demyelinating Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy type 1, Charcot-Marie-Tooth type 1

46 clinical trials for this condition and its sub-types, 4 tagged with Charcot-Marie-Tooth disease type 1 itself.