Klippel–Trénaunay–Weber Syndrome

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.

Read more about Klippel–Trénaunay–Weber Syndrome:  Classification, Signs and Symptoms, Genetics, Treatment, History, Notable Cases

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