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Telangiectasia, Hereditary Hemorrhagic

"Telangiectasia, Hereditary Hemorrhagic" 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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An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA.


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This graph shows the total number of publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in UAMS Profiles by year, and whether "Telangiectasia, Hereditary Hemorrhagic" was a major or minor topic of these publications.
Bar chart showing 6 publications over 6 distinct years, with a maximum of 1 publications in 1995 and 2011 and 2013 and 2015 and 2020 and 2021
To see the data from this visualization as text, click here.