Familial joint laxity (Q57027): Difference between revisions
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A síndrome de Ehlers-Danlos (EDS) tipo 11 é um tipo de EDS caracterizada por hipermobilidade articular generalizada, muitas vezes complicada por luxação de grandes articulações, particularmente do ombro, mas em alguns casos da rótula. Luxação congênita do quadril também foi frequentemente relatada. | |||
| description / en | description / en | ||
Ehlers-Danlos syndrome (EDS) type 11, is a type of EDS characterised by generalised joint hypermobility often complicated by dislocation of major joints, particularly the shoulder but in some cases the kneecap. Congenital hip dislocation has also been frequently reported. | |||
Revision as of 04:42, 14 August 2026
Ehlers-Danlos syndrome (EDS) type 11, is a type of EDS characterised by generalised joint hypermobility often complicated by dislocation of major joints, particularly the shoulder but in some cases the kneecap. Congenital hip dislocation has also been frequently reported.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1609305399 |
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| English | Familial joint laxity |
Ehlers-Danlos syndrome (EDS) type 11, is a type of EDS characterised by generalised joint hypermobility often complicated by dislocation of major joints, particularly the shoulder but in some cases the kneecap. Congenital hip dislocation has also been frequently reported. |
