X-linked distal spinal muscular atrophy type 3

MONDO:0010338

X-linked distal spinal muscular atrophy type 3 is a rare distal hereditary motor neuropathy characterized by slowly progressive atrophy and weakness of distal muscles of hands and feet with normal deep tendon reflexes or absent ankle reflexes and minimal or no sensory loss, sometimes mild proximal weakness in the legs and feet and hand deformities in males.

Also known as: ATP7A spinal muscular atrophy, ATP7A-related distal motor neuropathy, DSMAX, SMAX3, X-linked dHMN type 3, X-linked dHMN3, X-linked dSMA type 3, X-linked dSMA3

15 clinical trials for this condition and its sub-types, 0 tagged with X-linked distal spinal muscular atrophy type 3 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by