Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation (Q86057): Difference between revisions
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A distrofia muscular de cinturas (LGMD) 2H 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. LGMD 2H é transmitido como uma forma autossômica recessiva. | |||
| description / en | description / en | ||
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. | |||
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. |
