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Klippel-Trenaunay-Weber Syndrome

"Klippel-Trenaunay-Weber Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

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A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.


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This graph shows the total number of publications written about "Klippel-Trenaunay-Weber Syndrome" by people in UAMS Profiles by year, and whether "Klippel-Trenaunay-Weber Syndrome" was a major or minor topic of these publications.
Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 1993 and 2019
To see the data from this visualization as text, click here.
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