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Up to: Congenital nervous system disorder · Muscular dystrophy, limb-girdle, autosomal dominant · Myofibrillar myopathy · Autosomal dominant distal myopathy
Myofibrillar myopathy 3
A rare, late adult-onset myofibrillar myopathy characterized by progressive distal muscle weakness associated with peripheral neuropathy and hyporeflexia. Ambulation may be lost within a few years.
This condition has no sub-types.