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Autosomal recessive limb-girdle muscular dystrophy type 2Y
rareAutosomal recessive limb-girdle muscular dystrophy type 2Y (LGMD2Y) is a form of limb-girdle muscular dystrophy, presenting in the first or second decades of life, characterized by slowly progressive proximal and distal muscle weakness and atrophy. Additional manifestations include contractures of the proximal and distal interphalangeal hand joints, rigid spine, restricted pulmonary function, and mild cardiomyopathy.
- Identifiers
- MONDO:0014900 OMIM:617072Orphanet:424261
- Part of
- TOR1AIP1-related myopathyAutosomal recessive limb-girdle muscular dystrophyCongenital nervous system disorder
- Also known as
- autosomal recessive limb-girdle muscular dystrophy caused by mutation in TOR1AIP1 · autosomal recessive muscular dystrophy due to LAP1B deficiency · autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency · LGMD2Y · muscular dystrophy with progressive weakness, distal contractures and rigid spine
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