Klippel-Trénaunay syndrome (Q93467)
From determinar.ia.br - Determine suas informações
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 |
||
| 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 . |
Statements
CID11:ID_1477539224
0 references
