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Charcot-Marie-Tooth disease type 1

ORPHA:65753

Definition

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.

Prevalence
1-5 / 10 000
Inheritance
Autosomal dominant
Age of onset
Adolescent, Adult, Childhood, Infancy