A rare myopathy characterized by weakness of the muscles of the anterior compartment of lower limbs. Described as a more severe tibial muscular dystrophy phenotype, distal titinopathy is associated with earlier onset and progression to include soleus muscle and proximal muscles.
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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
Emery-Dreifuss-like muscular dystrophy
MONDO:0100496
titinopathy with congenital contractures
MONDO:0100497