Charcot-Marie-Tooth disease axonal type 2L
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Sign InDescription
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. In the single family reported to date, CMT2L onset is between 15 and 33 years. Patients present with a symmetric distal weakness of legs and occasionally of the hands, absent or reduced tendon reflexes, distal legs sensory loss and frequently a pes cavus. Progression is slow.
Mode of Inheritance
- Autosomal dominant inheritance
- Heterogeneous
VARIANTS
85