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Feb 12, 2022 · Klippel-Trenaunay (klih-PEL tray-no-NAY) syndrome ― also called KTS ― is a rare disorder found at birth (congenital) involving problems in the development of certain blood vessels, soft tissues (such as skin and muscles), bones and sometimes the lymphatic system.

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Oct 8, 2020 · Klippel Trenaunay syndrome (KTS) is a vascular malformation syndrome comprising varying involvement of cutaneous capillaries, veins, and lymphatics with hypertrophy of soft tissue and bones of the affected limb. This syndrome is also referred to as capillary-lymphatic-venous malformation (CLVM), reflecting the changes seen in those vessels.

Klippel-Trenaunay syndrome (KTS) is a rare congenital (present at birth) condition. It causes a port-wine stain birthmark and problems with veins, bones or soft tissues. Healthcare providers often identify KTS early and may diagnose it before a newborn leaves the hospital. With treatment, most people with KTS can live a typical life.

Klippel-Trenaunay syndrome, also called KTS or KT syndrome, is a rare venous malformation disorder. KTS affects how blood and lymph vessels develop in a baby before birth. Klippel Trenaunay Weber syndrome is an older name for the condition.

Klippel-Trenaunay syndrome (KTS) is a complex congenital disorder defined as the triad of capillary malformation, venous malformation, and limb overgrowth, with or without lymphatic malformation [1,2].

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Jan 6, 2016 · Klippel-Trenaunay syndrome (KTS) (OMIM # 149000) is a combination of slow-flow vascular malformations (capillary, lymphatic, and venous) in an overgrown limb. KTS is the prototype of complex overgrowth disorder associated with vascular anomalies and is the most common of these disorders.

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