Klippel-Trenaunay-Weber syndrome; KTS; Angio-osteohypertrophy; Nevus varicosus osteohypertrophicus syndrome; Hemangiectasia hypertrophicans; Nevus verucosus hypertrophicans
Causes, incidence, and risk factors
Most cases of Klippel-Trenaunay syndrome occur for no apparent reason. However, a few cases are thought to be passed down through families (inherited), possibly as an autosomal dominant trait.
- Many port wine stains or other blood vessel problems, including dark spots on the skin.
- Varicose veins (may be seen in early infancy, but are more likely to be seen later in childhood or adolescence)
Other possible symptoms:
- Bleeding from the rectum
- Blood in the urine
Signs and tests
Persons with this condition may have excessive growth of bones and soft tissue. This occurs most commonly in the legs, but it also may affect the arms, face, head, or internal organs.
It may be helpful to join a support group in which members share common problems and concerns.
The following organizations provide further information on Klippel-Trenaunay syndrome:
- The Klippel-Trenaunay Syndrome Support Group --www.k-t.org
- Vascular Birthmarks Foundation -- www.birthmark.org
Most people with Klippel-Trenaunay syndrome do well, although the condition may affect their appearance. Some people have psychological problems from the condition.
There can sometimes be abnormal blood vessels in the abdomen, which need to be evaluated.
Garzon M, Huang J, Enjolras O, Frieden I. Vascular malformations. Part II: associated syndromes. J Am Acad Derm. 2007;56(4):541-564.
Reviewed by:Chad Haldeman-Englert, MD, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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