Also known as:
KTS, Klippel-Weber-Tr?naunay syndrome, CLVM
Klippel-Trénaunay syndrome (KTS) is a rare disorder that is present at birth (congenital) and is characterized by a triad of cutaneous capillary malformation ("port-wine stain"), lymphatic anomalies, and abnormal veins in association with variable overgrowth of soft tissue and bone.
KTS occurs most frequently in the lower limb and less commonly in the upper extremity and trunk. KTS equally affects males and females.
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