Klippel-Trénaunay syndrome (Q93467): Difference between revisions
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A síndrome de Klippel-Trenaunay (KTS) (OMIM 149000) é caracterizada por hipertrofia de membro, malformações capilares e malformações vasculares de fluxo lento do membro afetado. Difere da síndrome de Parkes-Weber, na qual a hipertrofia de membro e as malformações capilares estão associadas a malformações arteriovenosas de fluxo rápido e, em alguns casos, a mutações no gene RASA1. | |||
| description / en | description / en | ||
Klippel-Trenaunay syndrome (KTS) (OMIM 149000) is characterised by limb hypertrophy, capillary malformations and slow flow vascular malformations of the affected limb. It differs from Parkes-Weber syndrome in which limb hypertrophy and capillary malformations are associated with fast flow arteriovenous malformations and, in some cases, with mutations in the RASA1 gene . | |||
Revision as of 08:34, 16 August 2026
Klippel-Trenaunay syndrome (KTS) (OMIM 149000) is characterised by limb hypertrophy, capillary malformations and slow flow vascular malformations of the affected limb. It differs from Parkes-Weber syndrome in which limb hypertrophy and capillary malformations are associated with fast flow arteriovenous malformations and, in some cases, with mutations in the RASA1 gene .
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1477539224 |
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| English | Klippel-Trénaunay syndrome |
Klippel-Trenaunay syndrome (KTS) (OMIM 149000) is characterised by limb hypertrophy, capillary malformations and slow flow vascular malformations of the affected limb. It differs from Parkes-Weber syndrome in which limb hypertrophy and capillary malformations are associated with fast flow arteriovenous malformations and, in some cases, with mutations in the RASA1 gene . |
