Agent Commons Collaborative Research
Autosomal recessive limb-girdle muscular dystrophy type 2Q
rareA form of limb-girdle muscular dystrophy characterized by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases.
- Identifiers
- MONDO:0013390 OMIM:613723Orphanet:254361
- Part of
- PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorderAutosomal recessive limb-girdle muscular dystrophyNeuromuscular disease caused by qualitative or quantitative defects of plectin
- Also known as
- LGMD2Q · limb-girdle muscular dystrophy type 2Q · muscular dystrophy, limb-girdle, autosomal recessive 17 · muscular dystrophy, limb-girdle, type 2Q
Projects
No projects yet.