ABSTRACT Introduction: Klippel-Tranaunay syndrome is a rare congenital condition
characterized by skin angiomas with arteriovenous malformations and hypertrophy of the …

Introducción: El síndrome de Klippel Trenaunay es una enfermedad rara congénita que se
caracteriza por angiomas cutáneos con malformaciones arterio-venosas e hipertrofia de los …

Failed Attempt of Total Hip Arthroplasty in a Patient with K... : JBJS Case Connector Failed
Attempt of Total Hip Arthroplasty in a Patient with Klippel-Trenaunay Syndrome: A Case …

Discussion Klippel–Trenaunay syndrome has 3 essential features: cutaneous
hemangiomas, varicose veins and hypertophy of the involved limbs in length or girth, or …

Klippel-Trenaunay syndrome (KTS) is a triad of cutaneous hemangiomas, varicose veins,
and localized hypertrophy of soft tissue and bone. Orthopedic surgical intervention may be …

Our experience with Klippel-Trenaunay syndrome (KTS), a rare congenital malformation,
has increased considerably in recent years and now includes 144 patients (65 male and 79 …

The Klippel-Trenaunay syndrome is a rare syndrome of uncertain etiology. The
characteristic elements are flat angiomatosis, hypertrophy of soft tissue and bone tissue and …

Klippel-Trenaunay syndrome (KTS) is a rare complex vascular congenital malformation. The
characteristic triad is an association of a cutaneous capillary angioma of a limb, venous …

Klippel-Trenaunay Syndrome (KTS) is a rare congenital disorder characterized by a triad of
capillary malformation with port-wine stain, varicose veins, or venous malformation of the …

Abstract Klippel–Trenaunay Syndrome is a congenital disorder with a rare incidence of 3-
5/1, 00,000. It is characterized by a triad of capillary malformation (hemangioma or port-wine …