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 …

Klippel-Trenaunay syndrome (KTS) is a rare congenital, vascular disorder affecting one or
more limbs. The syndrome is characterized by capillary malformations, soft tissue or bony …

Klippel-Trenaunay syndrome (KTS) is characterized by the classic triad of capillary
malformations manifesting as a" port-wine stain", venous varicosities, and bone and/or soft …

Klippel–Trenaunay syndrome (KTS) is a rare congenital disorder with an incidence of 1 in
100,000. It is characterized by a triad of capillary malformations (hemangiomas) or port-wine …

We aim to review the imaging findings of Klippel-Trenaunay syndrome. This disorder
characterized clinically by a triad of capillary malformations manifesting as a port-wine stain …

Klippel-Trenaunay syndrome (KTS) is a rare genetic syndrome comprising an abnormal
development of soft tissues and the lymphovascular system with bony overgrowth, venous …

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 …

A case of Klippel–Trenaunay syndrome in a 20-year-old girl was described in this article.
The clinical data showed that she had suffered from circuitous and dilated veins in her right …

Klippel-Trenaunay syndrome is a rare congenital vascular disease. The pathogenesis of this
syndrome is unclear, but it is thought that most cases are the result of somatic mutations that …

Background We present a series of three cases of Klippel-Trenaunay syndrome (KTS)
presenting with unilateral lower limb involvement demonstrating a wide range of radiological …