CPN3 (medical condition): An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the Calpain-3 gene.
See also:
Limb-Girdle muscular dystrophy type 2A:
»Introduction: Limb-Girdle muscular dystrophy type 2A
»Symptoms of Limb-Girdle muscular dystrophy type 2A
CPN3: Another name for Limb-Girdle muscular dystrophy type 2A (or close medical condition association).
»Introduction: Limb-Girdle muscular dystrophy type 2A
»Symptoms of Limb-Girdle muscular dystrophy type 2A
Some of the symptoms of CPN3 incude:
See full list of 6 symptoms of CPN3 (Limb-Girdle muscular dystrophy type 2A)
These medical disease topics may be related to CPN3:
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