/Charcot-Marie-Tooth disease type 1B

Charcot-Marie-Tooth disease type 1B

Rare Disease

MONDO:0007307

Also Known As

CMT1BCharcot-Marie-Tooth disease slow nerve conduction type linked to DuffyCharcot-Marie-Tooth disease type 1 caused by mutation in MPZCharcot-Marie-Tooth disease, type 1BCharcot-Marie-Tooth neuropathy type 1BHMSN IBHMSN1BMPZ Charcot-Marie-Tooth disease type 1autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1Bhereditary motor and sensory neuropathy IBCMT 1BCharcot Marie Tooth disease type 1BCharcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1BCharcot-Marie-Tooth disease, demyelinating, type 1BCharcot-Marie-Tooth disease, slow nerve conduction type, linked to DuffyCharcot-Marie-Tooth neuropathy, type 1BHMSN 1BHMSN1hereditary motor and sensory neuropathy 1hereditary motor and sensory neuropathy 1B

Definition

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.