Limb-girdle muscular dystrophy 1B, lamin myopathy (Q84642): Difference between revisions
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A distrofia muscular de cinturas autossômica dominante tipo 1B é um tipo 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. O LGMD 1B é caracterizado por anormalidades da condução cardíaca com cardiomiopatia dilatada. | |||
| description / en | description / en | ||
Autosomal dominant limb-girdle muscular dystrophy type 1B 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. LGMD 1B is characterised by cardiac conduction abnormalities with dilated cardiomyopathy. | |||
Revision as of 09:59, 15 August 2026
Autosomal dominant limb-girdle muscular dystrophy type 1B 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. LGMD 1B is characterised by cardiac conduction abnormalities with dilated cardiomyopathy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_984625909 |
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| English | Limb-girdle muscular dystrophy 1B, lamin myopathy |
Autosomal dominant limb-girdle muscular dystrophy type 1B 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. LGMD 1B is characterised by cardiac conduction abnormalities with dilated cardiomyopathy. |
