Understanding Klippel-Trenaunay Syndrome

Klippel-Trenaunay Syndrome (KTS) is a rare congenital disorder characterized by port-wine stains, abnormal growth of bones and soft tissues, and vein malformations. This condition requires specialized medical care and management to address its complex symptoms and improve the quality of life for those affected.

What is Klippel-Trenaunay Syndrome? Klippel Trenaunay syndrome is a rare and complex combined vascular malformation that is present at birth. By definition, it includes evidence of malformations involving every vascular component except arteries. In addition, overgrowth of the involved extremity is common.

Capillary Malformations: Symptoms and Treatment Options Localized or diffuse capillary malformations (port-wine stains) can overly areas of venous and lymphatic malformations. Overgrowth of the limb will include all tissue types including muscle, bone, joints, and nerves. Internal organs may also be affected.

What is Klippel-Trenaunay Syndrome?

As with other types of vascular malformation, treatment is typically directed at symptoms that are present:

Limitation of movement or decreased function

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Schedule a consultation with Dr. Panossian — in person or virtual — to discuss your treatment options for klippel-trenaunay syndrome and begin your journey toward improved care.

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