Catalog

Klippel-Trénaunay syndrome

No MMS code

Link to WHO Definition

Klippel-Trénaunay syndrome – http://id.who.int/icd/entity/1477539224

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 .