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Autosomal recessive limb-girdle muscular dystrophy type 2H
rareAutosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H) is a mild subtype of autosomal recessive limb girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness and wasting of the pelvic and shoulder girdles with onset that usually occurs during the second or third decade of life. Clinical presentation is variable and can include calf psuedohypertrophy, joint contractures, scapular winging, muscle cramping and/or facial and respiratory muscle involvement.
- Identifiers
- MONDO:0009683 OMIM:254110Orphanet:1878
- Part of
- Autosomal recessive limb-girdle muscular dystrophyNeuromuscular disease caused by qualitative or quantitative defects of TRIM32
- Also known as
- autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32 · LGMD2H · limb-girdle muscular dystrophy due to TRIM32 deficiency · limb-girdle muscular dystrophy type 2H · muscular dystrophy limb-girdle type 2H
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