Limb-girdle muscular dystrophy 1C, caveolin myopathy (Q84647): Difference between revisions
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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 |
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| 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. |
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CID11:ID_726171912
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dki-india-ID_726171912
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