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Autosomal recessive limb-girdle muscular dystrophy type 2F
rareAutosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuropsychomotor development is usually normal.
- Identifiers
- MONDO:0011028 OMIM:601287Orphanet:219
- Part of
- Autosomal recessive limb-girdle muscular dystrophyFamilial dilated cardiomyopathyQualitative or quantitative defects of delta-sarcoglycan
- Also known as
- autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCD · LGMD2F · limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency · limb-girdle muscular dystrophy type 2F · muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
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