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