Tags: Disease.
Klippel–Trénaunay–Weber syndrome often simply Klippel–Trénaunay syndrome (KTS) and sometimes angioosteohypertrophy syndrome and hemangiectatic hypertrophy is a rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain) venous and lymphatic malformations and soft-tissue hypertrophy of the affected limb.
