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 |
|---|
| 1997 | 0 | 1 | 1 |
| 2004 | 1 | 1 | 2 |
| 2006 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in Profiles.
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Rodgers SK, DeMauro C. Case 3: Diagnosis: hereditary hemorrhagic telangiectasia. Ultrasound Q. 2007 Mar; 23(1):70-3.
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Chung DY, Federle MP, Barrett JP, Sass DA. Hepatic hereditary hemorrhagic telangiectasia. Clin Gastroenterol Hepatol. 2006 Nov; 4(11):xx.
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Blumenthal BM, Slizofski W, Hoffman M. Technetium-99m-labeled RBC bleeding scan in a patient with Osler-Weber-Rendu Disease. Clin Nucl Med. 2004 Dec; 29(12):861-3.
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Jabbour P, Gault J, Awad IA. What genes can teach us about human cerebrovascular malformations. Clin Neurosurg. 2004; 51:140-52.
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Parenti DJ, Simelaro JP, Venditto MA. Hypoxemia and recurrent epistaxis in an 81-year-old woman. Hosp Pract (1995). 1997 Aug 15; 32(8):107-8, 115-6, 121.
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Siegel MB, Keane WM, Atkins JF, Rosen MR. Control of epistaxis in patients with hereditary hemorrhagic telangiectasia. Otolaryngol Head Neck Surg. 1991 Nov; 105(5):675-9.
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Wolper J, Laibson PR. Hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber disease) with filamentary keratitis. Arch Ophthalmol. 1969 Feb; 81(2):272-7.