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Up to: Syndromic disease · Autosomal recessive limb-girdle muscular dystrophy · Epidermolysis bullosa simplex · PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder · Neuromuscular disease caused by qualitative or quantitative defects of plectin
Epidermolysis bullosa simplex 5B, with muscular dystrophy
A basal subtype of epidermolysis bullosa simplex (EBS) characterized by generalized blistering associated with muscular dystrophy.
This condition has no sub-types.