Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Congenital nervous system disorder · Congenital myopathy · Distal myopathy · Neuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)
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.
This condition has no sub-types.