Limb-girdle muscular dystrophy 1C, caveolin myopathy (Q84647): Difference between revisions

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Latest revision as of 09:59, 15 August 2026

Autosomal dominant limb-girdle muscular dystrophy (LGMD) type 1C is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by childhood onset. It has not been associated with cardiac problems.

Language	Label	Description	Also known as
default for all languages	ID_726171912
English	Limb-girdle muscular dystrophy 1C, caveolin myopathy	Autosomal dominant limb-girdle muscular dystrophy (LGMD) type 1C is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by childhood onset. It has not been associated with cardiac problems.