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.
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.
| Descriptor ID |
D013683
|
| MeSH Number(s) |
C14.907.454.900 C14.907.823.780 C15.378.463.515.900 C16.131.240.850.968
|
| Concept/Terms |
Telangiectasia, Hereditary Hemorrhagic- Telangiectasia, Hereditary Hemorrhagic
- Hemorrhagic Telangiectasia, Hereditary
- Rendu-Osler-Weber
- Rendu Osler Weber
- Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
- Telangiectasia, Hereditary Hemorrhagic, Type 1
- Osler-Rendu Disease
- Osler Rendu Disease
- Osler-Rendu-Weber Disease
- Osler Rendu Weber Disease
- Hereditary Hemorrhagic Telangiectasia
- Osler's Disease
- Disease, Osler's
- Osler Disease
- Osler-Weber-Rendu Syndrome
- Osler Weber Rendu Syndrome
- Weber-Osler
- Weber Osler
|
Below are MeSH descriptors whose meaning is more general than "Telangiectasia, Hereditary Hemorrhagic".
Below are MeSH descriptors whose meaning is more specific than "Telangiectasia, Hereditary Hemorrhagic".
This graph shows the total number of publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in this website by year, and whether "Telangiectasia, Hereditary Hemorrhagic" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 4 | 0 | 4 |
| 2018 | 5 | 0 | 5 |
| 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in Profiles.
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Pulmonary Abnormalities in Liver Disease: Relevance to Transplantation and Outcome. Hepatology. 2021 09; 74(3):1674-1686.
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Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations. BMJ Case Rep. 2021 Jan 08; 14(1).
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Diagnostic testing for SARS-CoV-2 infection in HHT patients: nasopharyngeal versus oropharyngeal swab. Orphanet J Rare Dis. 2020 12 18; 15(1):350.
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Hereditary hemorrhagic telangiectasia and COVID-19. Rev Soc Bras Med Trop. 2020; 53:e20200785.
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Angiogenesis, hereditary hemorrhagic telangiectasia and COVID-19. Angiogenesis. 2021 02; 24(1):13-15.
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Mental health and counseling intervention for hereditary hemorrhagic telangiectasia (HHT) during the COVID-19 pandemic: perspectives from Italy. Eur Rev Med Pharmacol Sci. 2020 Oct; 24(19):10225-10227.
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Hereditary haemorrhagic telangiectasia: A disease not to be forgotten during the COVID-19 pandemic. J Thromb Haemost. 2020 07; 18(7):1799-1801.
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Laryngeal hereditary hemorrhagic telangiectasia. Ear Nose Throat J. 2018 Dec; 97(12):388.
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Pentraxin 3 level is elevated in hereditary hemorrhagic telangiectasia and reflects the severity of disease-associated epistaxis. Laryngoscope. 2019 01; 129(1):E44-E49.
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Pulmonary Arteriovenous Malformations: Safety and Efficacy of Microvascular Plugs. AJR Am J Roentgenol. 2018 11; 211(5):1135-1143.