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Autosomal recessive limb-girdle muscular dystrophy type 2C
rareAutosomal recessive limb-girdle muscular dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported.
- Identifiers
- MONDO:0009677 OMIM:253700Orphanet:353
- Part of
- Autosomal recessive limb-girdle muscular dystrophyFamilial dilated cardiomyopathyQualitative or quantitative defects of gamma-sarcoglycan
- Also known as
- autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCG · DMDA1 · gamma-sarcoglycanopathy · LGMD2C · limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
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