Limb-girdle muscular dystrophy 1E, gene mapped to 7q (Q84651): Difference between revisions
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A distrofia muscular de cinturas tipo 1E (LGMD1E) pertence a 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 pelo início no final da idade adulta, possível disfagia e não evidente anormalidades cardíacas. | |||
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Autosomal dominant limb-girdle muscular dystrophy type 1D 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 1D is transmitted as an autosomal dominant form. | |||
Revision as of 09:59, 15 August 2026
Autosomal dominant limb-girdle muscular dystrophy type 1D 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 1D is transmitted as an autosomal dominant form.
| Language | Label | Description | Also known as |
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| default for all languages | ID_586397197 |
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| English | Limb-girdle muscular dystrophy 1E, gene mapped to 7q |
Autosomal dominant limb-girdle muscular dystrophy type 1D 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 1D is transmitted as an autosomal dominant form. |
