Charcot-Marie-Tooth disease type 1B

A sensorineural peripheral polyneuropathy affecting approximately 1 in 2,500 individuals, and is the most common inherited disorder of the peripheral nervous system. Autosomal dominant, autosomal recessive, and X-linked forms have been recognized.

Also known as: CMT1B, Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ, Charcot-Marie-Tooth disease, type 1B, HMSN IB, HMSN1B, MPZ Charcot-Marie-Tooth disease type 1, CMT 1B, Charcot Marie Tooth disease type 1B

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