Charcot-Marie-Tooth disease type 2A1

Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (CMT2A1) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2A presents with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor.

Also known as: CMT2A, CMT2A1, Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B, Charcot-Marie-Tooth disease type 2A, Charcot-Marie-Tooth disease type 2A1, Charcot-Marie-Tooth disease, type 2A1, HMSN IIA1, HMSN2A1

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