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Up to: Autosomal recessive limb-girdle muscular dystrophy · Muscular dystrophy-dystroglycanopathy, type C · Myopathy caused by variation in POMT2 · Qualitative or quantitative defects of protein O-mannosyltransferase 2
Autosomal recessive limb-girdle muscular dystrophy type 2N
Autosomal recessive limb-girdle muscular dystrophy type 2N (LGMD2N) is a form of limb-girdle muscular dystrophy characterized by proximal weakness (manifesting as slowness in running) presenting in infancy, along with calf hypertrophy, mild lordosis, scapular winging and normal intelligence or mild intellectual disability.
This condition has no sub-types.