Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation (Q86057): Difference between revisions
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Revision as of 11:25, 15 August 2026
Limb girdle muscular dystrophy (LGMD) 2H 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 2H is transmitted as an autosomal recessive form.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2020366790 |
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| English | Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation |
Limb girdle muscular dystrophy (LGMD) 2H 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 2H is transmitted as an autosomal recessive form. |
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CID11:ID_2020366790
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dki-india-ID_2020366790
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