Limb-girdle muscular dystrophy 1D, gene mapped to 6q23 (Q84668): Difference between revisions
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A distrofia muscular de cinturas autossômica dominante tipo 1D 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. O LGMD 1D é transmitido como uma forma autossômica dominante. | |||
| description / en | description / en | ||
Limb girdle muscular dystrophy, type1E (LGMD1E) belongs to 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 onset in late adulthood, possible dysphagia and no evident cardiac abnormalities. | |||
Revision as of 10:01, 15 August 2026
Limb girdle muscular dystrophy, type1E (LGMD1E) belongs to 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 onset in late adulthood, possible dysphagia and no evident cardiac abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2145132790 |
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| English | Limb-girdle muscular dystrophy 1D, gene mapped to 6q23 |
Limb girdle muscular dystrophy, type1E (LGMD1E) belongs to 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 onset in late adulthood, possible dysphagia and no evident cardiac abnormalities. |
