Charcot-Marie-Tooth disease type 2E
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Sign InDescription
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, with onset in the first to 6th decade with a gait anomaly and a leg weakness that reaches the arms secondarily. Tendon reflexes are reduced or absent and, after years, all patients have a pes cavus. Other signs may be present, including hearing loss and postural tremor.
Mode of Inheritance
- Autosomal dominant inheritance
VARIANTS
166