A congenital disorder that is characterized by a triad of capillary malformations (hemangioma), venous malformations (arteriovenous fistula), 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.


Leave a message about 'Klippel-Trenaunay-Weber Syndrome'


We do not evaluate or guarantee the accuracy of any content in this site. Click here for the full disclaimer.