Myofibrillar myopathy 3

MONDO:0012215

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.

Also known as: LGMD1A, MYOT autosomal dominant distal myopathy, MYOT autosomal dominant limb-girdle muscular dystrophy, MYOT-related myofibrillar myopathy, autosomal dominant distal myopathy caused by mutation in MYOT, autosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOT, autosomal dominant limb-girdle muscular dystrophy type 1A, distal myotilinopathy

8 clinical trials for this condition and its sub-types, 0 tagged with Myofibrillar myopathy 3 itself.

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↑ Congenital nervous system disorder (287) ↑ Muscular dystrophy, limb-girdle, autosomal dominant (4) ↑ Myofibrillar myopathy (3) ↑ Autosomal dominant distal myopathy (0)

Including sub-types (8) Tagged with Myofibrillar myopathy 3 (0)

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