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Klippel-Trenaunay Syndrome Reviewed 01-28-2003 Get Web page suited for printing Email this to a friend or colleague Studies with patients Table of Contents (click to jump to sections) What is Klippel-Trenaunay Syndrome?Is there any treatment? What is the prognosis? What research is being done? Organizations What is Klippel-Trenaunay Syndrome? Klippel-Trenaunay syndrome (KTS) is a congenital circulatory disorder characterized by hemiangiomas (abnormal benign growths on the skin consisting of masses of blood vessels), arteriovenous abscesses, and varicose veins, usually on the limbs. The affected limbs may be enlarged and warmer than normal. Fused toes or fingers, or extra toes or fingers, may be present. Bleeding may occur, often as a result of a rectal or vaginal tumor. The cause of the disorder is unknown. A similar port-wine stain disorder in which individuals have vascular anomalies and limb enlargement is Sturge-Weber syndrome. These patients may experience seizures and mental deficiency. Is there any treatment? What is the prognosis? What research is being done? Vascular Birthmarks Foundation
Sturge-Weber Foundation
National Organization for Rare Disorders (NORD)
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