Charcot-Marie-Tooth disease axonal type 2N

Autosomal dominant Charcot-Marie-Tooth disease type 2N (CMT2N) is a mild form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal legs sensory loss and weakness that can be asymmetric. Tendon reflexes are reduced in the knees and absent in ankles. Progression is slow.

Also known as: AARS Charcot-Marie-Tooth disease type 2, CMT2N, Charcot-Marie-Tooth disease type 2 caused by mutation in AARS, autosomal dominant Charcot-Marie-Tooth disease type 2N, Charcot-Marie-Tooth disease type 2N, Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2N, Charcot-Marie-Tooth disease, axonal, type 2N, Charcot-Marie-Tooth neuropathy, axonal, type 2N

9 clinical trials for this condition and its sub-types.