Charcot-Marie-Tooth disease type 4G

Charcot-Marie-Tooth disease type 4G (CMT4G) is a subtype of Charcot-Marie-Tooth disease type 4 characterized by early childhood onset of progressive distal muscle weakness and atrophy, delayed motor development, prominent distal sensory impairment, areflexia, moderately reduced nerve conduction velocities, and foot and hand deformities in Balkan (Russe) Gypsies.

Also known as: CMT4G, Charcot-Marie-Tooth disease type 4 caused by mutation in HK1, HK1 Charcot-Marie-Tooth disease type 4, HMSNR, hereditary motor and sensory neuropathy, Russe type, Charcot-Marie-Tooth disease, autosomal recessive, type 4G, Charcot-Marie-Tooth disease, type 4G, Charcot-Marie-Tooth neuropathy, type 4G

10 clinical trials for this condition and its sub-types, 0 tagged with Charcot-Marie-Tooth disease type 4G itself.