Limb-girdle muscular dystrophy 2E, beta-sarcoglycan deficiency (Q86055): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
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. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/867128398 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_867128398 | |||||||||||||||
| Property / CURIE: CID11:ID_867128398 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_867128398 | |||||||||||||||
| Property / Canary Token: dki-india-ID_867128398 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
||
| 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
0 references
dki-india-ID_867128398
0 references
Concluído
0 references
13 August 2026
0 references
