Limb-girdle muscular dystrophy 2E, beta-sarcoglycan deficiency (Q86055): Difference between revisions
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13 August 2026
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Latest 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 |
|---|---|---|---|
| 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. |
Statements
CID11:ID_867128398
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dki-india-ID_867128398
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Concluído
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13 August 2026
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