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.
MeSH information
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.


Publications
This graph shows the total number of publications written about "Klippel-Trenaunay-Weber Syndrome" by people in this website by year, and whether "Klippel-Trenaunay-Weber Syndrome" was a major or minor topic of these publications.
Bar chart showing 186 publications over 26 distinct years, with a maximum of 15 publications in 2009 and 2010
To see the data from this visualization as text, click here.