Limb-girdle muscular dystrophy 1A, myotilin myopathy (Q84639): Difference between revisions
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A distrofia muscular de cinturas autossômica dominante tipo 1A pertence a um grupo de distúrbios de fraqueza muscular progressiva, geneticamente determinados, nos quais a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida. O LGMD 1A é caracterizado por disartria e não foi associado a problemas cardíacos, com início na idade adulta jovem. | |||
| description / en | description / en | ||
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. | |||
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 |
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| default for all languages | ID_172327936 |
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| 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. |
