ICD Q87.2ORPHA:90308KTS

Klippel-Trénaunay Syndrome

Klippel-Trénaunay syndrome is a rare condition in which blood and lymph vessels do not form normally in one part of the body, usually a leg. It typically causes a port-wine stain on the skin, swollen or varicose veins, lymphatic swelling, and overgrowth of the affected limb. Care is shared between specialists and may include compression garments, sclerotherapy, laser treatment, surgery and targeted medicines, along with pain and mobility support.

186
Articles
9
Trials (1 AU)
Updated
24 September 2026
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Common Questions

What is Klippel-Trénaunay Syndrome?

Klippel-Trénaunay syndrome is a rare condition in which blood and lymph vessels do not form normally in one part of the body, usually a leg. It typically causes a port-wine stain on the skin, swollen or varicose veins, lymphatic swelling, and overgrowth of the affected limb. Care is shared between specialists and may include compression garments, sclerotherapy, laser treatment, surgery and targeted medicines, along with pain and mobility support.

How many clinical trials are available for Klippel-Trénaunay Syndrome?

RareWays currently indexes 9 clinical trials for Klippel-Trénaunay Syndrome, of which 4 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Klippel-Trénaunay Syndrome come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.