Limb-girdle muscular dystrophy 1F, gene mapped to 7q32.1-32.2 (Q84652): Difference between revisions
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A distrofia muscular de cinturas tipo 1F (LGMD1F) é uma forma autossômica dominante de LGMD, um grupo de distúrbios de fraqueza muscular progressiva, geneticamente determinados, em que a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida e é caracterizada por fraqueza do músculos pélvicos e ombros | |||
| description / en | description / en | ||
Limb girdle muscular dystrophy, type 1F (LGMD1F) is an autosomal dominant form 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 weakness of the pelvic and shoulder muscles | |||
Revision as of 09:59, 15 August 2026
Limb girdle muscular dystrophy, type 1F (LGMD1F) is an autosomal dominant form 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 weakness of the pelvic and shoulder muscles
| Language | Label | Description | Also known as |
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| default for all languages | ID_2102590721 |
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| English | Limb-girdle muscular dystrophy 1F, gene mapped to 7q32.1-32.2 |
Limb girdle muscular dystrophy, type 1F (LGMD1F) is an autosomal dominant form 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 weakness of the pelvic and shoulder muscles |
