Ehlers-Danlos syndrome, hypermobile type (Q86803): Difference between revisions
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A síndrome de Ehlers-Danlos, forma hipermóvel (anteriormente SED tipo III) é a forma mais frequente de SED e é caracterizada por hiperfrouxidão articular generalizada, que frequentemente é bastante grave (escore de Beighton acima de 5) e graus variáveis de hiperextensibilidade da pele. | |||
| description / en | description / en | ||
Ehlers-Danlos syndrome, hypermobile form (formerly EDS type III) is the most frequent form of EDS and is characterised by generalised joint hyperlaxity, which is often quite severe (Beighton score above 5) and variable degrees of skin hyperextensibility. | |||
Revision as of 12:21, 15 August 2026
Ehlers-Danlos syndrome, hypermobile form (formerly EDS type III) is the most frequent form of EDS and is characterised by generalised joint hyperlaxity, which is often quite severe (Beighton score above 5) and variable degrees of skin hyperextensibility.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_24232012 |
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| English | Ehlers-Danlos syndrome, hypermobile type |
Ehlers-Danlos syndrome, hypermobile form (formerly EDS type III) is the most frequent form of EDS and is characterised by generalised joint hyperlaxity, which is often quite severe (Beighton score above 5) and variable degrees of skin hyperextensibility. |
