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Autosomal dominant Charcot-Marie-Tooth disease type 2J

ORPHA:99943· ICD-10 G60.0

Definition

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a relatively late onset, pupillary abnormalities and deafness, in most patients, associated with distal weakness and muscle atrophy.

Inheritance
Autosomal dominant
Age of onset
Adult