Limb-girdle muscular dystrophy 2E, beta-sarcoglycan deficiency (Q86055): Difference between revisions
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A distrofia muscular de cinturas autossômica recessiva tipo 2E 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 2E é transmitido como uma forma autossômica recessiva e é caracterizada por asa escapular e hipertrofia da panturrilha. | |||
| description / en | description / en | ||
Autosomal recessive limb-girdle muscular dystrophy type 2E 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 2E is transmitted as an autosomal recessive form and is characterised by scapular winging and calf hypertrophy. | |||
Revision as of 11:25, 15 August 2026
Autosomal recessive limb-girdle muscular dystrophy type 2E 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 2E is transmitted as an autosomal recessive form and is characterised by scapular winging and calf hypertrophy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_867128398 |
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| English | Limb-girdle muscular dystrophy 2E, beta-sarcoglycan deficiency |
Autosomal recessive limb-girdle muscular dystrophy type 2E 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 2E is transmitted as an autosomal recessive form and is characterised by scapular winging and calf hypertrophy. |
