Limb-girdle muscular dystrophy 1A, myotilin myopathy (Q84639): Difference between revisions
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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 |
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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. |
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CID11:ID_172327936
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