Charcot-Marie-Tooth disease type 2I

Autosomal dominant Charcot-Marie-Tooth disease type 2I (CMT2I) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a late onset with severe sensory loss (paresthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes.

Also known as: CMT2I, Charcot-Marie-Tooth disease, type 2I, CMT 2I, Charcot Marie Tooth disease type 2I, Charcot-Marie-Tooth disease, axonal, type 2I, Charcot-Marie-Tooth neuropathy, type 2I, autosomal dominant Charcot-Marie-Tooth disease type 2I

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