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Up to: Autosomal recessive limb-girdle muscular dystrophy · PLEC-related muscular dystrophy-epidermolysis bullosa simplex spectrum disorder · Neuromuscular disease caused by qualitative or quantitative defects of plectin
Autosomal recessive limb-girdle muscular dystrophy type 2Q
A 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.
This condition has no sub-types.