A rare inherited muscular dystrophy characterized by the coexistence of limb-girdle weakness and early-onset diffuse joint contractures without cardiomyopathy.
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autosomal recessive limb-girdle muscular dystrophy type 2J
MONDO:0012127
early-onset myopathy with fatal cardiomyopathy
MONDO:0012714
autosomal recessive centronuclear myopathy
MONDO:0015705
classic multiminicore myopathy
MONDO:0017939
autosomal recessive distal titinopathy
MONDO:0100495
titinopathy with congenital contractures
MONDO:0100497