MYH7-related skeletal myopathy

A rare autosomal dominant distal myopathy characterized by preferential weakness of the great toe, ankle dorsiflexor, finger extensor and neck flexor. Progression is slow with variations in age of onset, severity, weakness, cardiac, and respiratory involvement.

Also known as: Laing distal myopathy, MPD1, MYH7-related skeletal myopathy, distal myopathy type 1, myopathy distal, type 1, myopathy, distal, 1, myopathy, distal, early-onset, autosomal dominant, myopathy, distal, type 1

6 clinical trials for this condition and its sub-types, 0 tagged with MYH7-related skeletal myopathy itself.