Definición:
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.
Sinónimos:
Sindrome de Klippel-Trenaunay-Weber /
Enfermedad de Klippel-Trenaunay /