 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
- Hereditary Hemorrhagic Telangiectasia
- Telangiectasia, Hereditary Hemorrhagic, Type 1
- Osler-Weber-Rendu Syndrome
- Osler Weber Rendu Syndrome
- Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber
- Osler-Rendu Disease
- Osler Rendu Disease
- Osler-Rendu-Weber Disease
- Osler Rendu Weber Disease
|
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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1989 | 1 | 0 | 1 | | 1994 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1998 | 2 | 0 | 2 | | 2001 | 0 | 1 | 1 | | 2004 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2009 | 0 | 1 | 1 | | 2011 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Telangiectasia, Hereditary Hemorrhagic" by people in Profiles.
-
Chowdhry SA, Ponsky DC, Hsu DP. Treatment of a nasal vascular malformation in a patient with Osler-Weber-Rendu syndrome via percutaneous N-butyl 2-cyanoacrylate embolization: case report and review of the literature. J Otolaryngol Head Neck Surg. 2011 Apr; 40(2):E11-4.
-
Lee M, Sze DY, Bonham CA, Daugherty TJ. Hepatic arteriovenous malformations from hereditary hemorrhagic telangiectasia: treatment with liver transplantation. Dig Dis Sci. 2010 Nov; 55(11):3059-62.
-
Leblanc GG, Golanov E, Awad IA, Young WL. Biology of vascular malformations of the brain. Stroke. 2009 Dec; 40(12):e694-702.
-
Seike Y, Sato H, Nagashima M, Hori T, Ishitoya H, Hibino N, Tomino T, Nakata T. [Aortic valve replacement for the patient with Osler-Rendu-Weber disease]. Kyobu Geka. 2005 Dec; 58(13):1141-4.
-
Jabbour P, Gault J, Awad IA. What genes can teach us about human cerebrovascular malformations. Clin Neurosurg. 2004; 51:140-52.
-
Moussa RF, Wong JH, Awad IA. [Genetic factors related to intracranial arteriovenous malformations]. Neurochirurgie. 2001 May; 47(2-3 Pt 2):154-7.
-
Odorico JS, Hakim MN, Becker YT, Van der Werf W, Musat A, Knechtle SJ, D'Alessandro AM, Kalayoglu M. Liver transplantation as definitive therapy for complications after arterial embolization for hepatic manifestations of hereditary hemorrhagic telangiectasia. Liver Transpl Surg. 1998 Nov; 4(6):483-90.
-
Fulbright RK, Chaloupka JC, Putman CM, Sze GK, Merriam MM, Lee GK, Fayad PB, Awad IA, White RI. MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations. AJNR Am J Neuroradiol. 1998 Mar; 19(3):477-84.
-
Putman CM, Chaloupka JC, Fulbright RK, Awad IA, White RI, Fayad PB. Exceptional multiplicity of cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome). AJNR Am J Neuroradiol. 1996 Oct; 17(9):1733-42.
-
McAllister KA, Lennon F, Bowles-Biesecker B, McKinnon WC, Helmbold EA, Markel DS, Jackson CE, Guttmacher AE, Pericak-Vance MA, Marchuk DA. Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. J Med Genet. 1994 Dec; 31(12):927-32.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|