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Autosomal recessive limb-girdle muscular dystrophy type 2E
rareAutosomal recessive limb girdle muscular dystrophy type 2E (LGMD2E) is a subtype of autosomal recessive limb girdle muscular dystrophy characterized by a childhood to adolescent onset of progressive pelvic- and shoulder-girdle muscle weakness, particularly affecting the pelvic girdle (adductors and flexors of hip). Usually the knees are the earliest and most affected muscles. In advanced stages, involvement of the shoulder girdle (resulting in scapular winging) and the distal muscle groups are observed. Calf hypertrophy, cardiomyopathy, respiratory impairment, tendon contractures, scoliosis, and exercise-induced myoglobinuria may be observed.
- Identifiers
- MONDO:0011423 OMIM:604286Orphanet:119
- Part of
- Autosomal recessive limb-girdle muscular dystrophyFamilial dilated cardiomyopathyQualitative or quantitative defects of beta-sarcoglycan
- Also known as
- autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCB · beta-sarcoglycan limb-girdle muscular dystrophy · beta-sarcoglycan-related LGMD R4 · beta-sarcoglycan-related limb-girdle muscular dystrophy R4 · LGMD due to beta-sarcoglycan deficiency
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