Beschreibung:
A congenital disorder that is characterized by a triad of capillary malformations (), venous malformations (), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.
Synonym(s):
Haemangiectasia hypertrophica /
Riesenwuchs, partieller angiektatischer /
Klippel-Trénaunay-Parkes-Weber-Syndrom /
Klippel-Trénaunay-Syndrom /