Autosomal dominant slowed nerve conduction velocity

Autosomal dominant slowed nerve conduction velocity is a hereditary demyelinating motor and sensory neuropathy characterized by slowed nerve conduction velocities, in the absence of clinically apparent neurological deficits, gait abnormalities or muscular atrophy, associated with a germline mutation in the ARGHEF10 gene.

Also known as: autosomal dominant slowed nerve conduction velocity, slowed nerve conduction velocity, AD, SNCV, slowed nerve conduction velocity, autosomal dominant

6 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant slowed nerve conduction velocity itself.