📂 Diseases
Klippel–Trénaunay–Weber syndrome — Definition
Klippel-Trénaunay-Weber sendromu / Klippel–Trénaunay–Weber syndrome
Clippel-Trénaunay-Weber syndrome is a rare vascular anomalies that are congenital and often affect a single limbs. This syndrome is characterized by red-mor color porto wine stain on the skin, excessive bone and soft tissue growth (hypertrofi) and varicose veins in the affected area. Different from the classic Clippel-Trénaunay syndrome, this variant also contains arteriovenous fistulas (normal connections between the aggressive and the tops). The disease is caused by a disorder in the vascular system during embryonic development and is intended for symptoms of treatment.
Frequently Asked Questions
❓ What is Klippel-Trénaunay-Weber sendromu?
Klippel-Trénaunay-Weber sendromu; clippel-Trénaunay-Weber syndrome is a rare vascular anomalies that are congenital and often affect a single limbs. This syndrome is characterized by red-mor color porto wine stain on the skin, excessive bone and soft tissue growth (hypertrofi) and varicose veins in the affected area. Different from the classic Clippel-Trénaunay syndrome, this variant also contains arteriovenous fistulas (normal connections between the aggressive and the tops). The disease is caused by a disorder in the vascular system during embryonic development and is intended for symptoms of treatment.
❓ What is Klippel–Trénaunay–Weber syndrome in Turkish?
The Turkish equivalent of "Klippel–Trénaunay–Weber syndrome" is Klippel-Trénaunay-Weber sendromu.
❓ Which medical field is Klippel-Trénaunay-Weber sendromu related to?
This term belongs to the Diseases category.