Limb-girdle muscular dystrophy 1A, myotilin myopathy (Q84639): Difference between revisions

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Latest revision as of 09:59, 15 August 2026

Autosomal dominant limb-girdle muscular dystrophy type 1A belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1A is characterised by dysarthria and has not been associated with cardiac problems, with onset in young adulthood.

Language	Label	Description	Also known as
default for all languages	ID_172327936
English	Limb-girdle muscular dystrophy 1A, myotilin myopathy	Autosomal dominant limb-girdle muscular dystrophy type 1A belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1A is characterised by dysarthria and has not been associated with cardiac problems, with onset in young adulthood.