 Tetralogy of Fallot
"Tetralogy of Fallot" 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.
A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS.
| Descriptor ID |
D013771
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| MeSH Number(s) |
C14.240.400.849 C14.280.400.849 C16.131.240.400.849
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| Concept/Terms |
Tetralogy of Fallot- Tetralogy of Fallot
- Tetralogy, Fallot's
- Tetralogy, Fallot
- Tetralogy, Fallots
- Fallot's Tetralogy
- Fallot Tetralogy
- Fallots Tetralogy
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Below are MeSH descriptors whose meaning is more general than "Tetralogy of Fallot".
Below are MeSH descriptors whose meaning is more specific than "Tetralogy of Fallot".
This graph shows the total number of publications written about "Tetralogy of Fallot" by people in this website by year, and whether "Tetralogy of Fallot" 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 |
|---|
| 2015 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Tetralogy of Fallot" by people in Profiles.
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?koric-Milosavljevic D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T, Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genet Med. 2021 10; 23(10):1952-1960.
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Chan SS, Whitehead KK, Kim TS, Fu GL, Keller MS, Fogel MA, Harris MA. Repaired tetralogy of Fallot with coexisting unrepaired partial anomalous pulmonary venous connection is associated with diminished right ventricular ejection fraction and more severe right ventricular dilation. Pediatr Radiol. 2015 Sep; 45(10):1465-71.
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Rodemoyer A, Kibiryeva N, Bair A, Marshall J, O'Brien JE, Bittel DC. A tissue-specific gene expression template portrays heart development and pathology. Hum Genomics. 2014 Mar 11; 8:6.
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Bittel DC, Zhou XG, Kibiryeva N, Fiedler S, O'Brien JE, Marshall J, Yu S, Liu HY. Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot. PLoS One. 2014; 9(1):e87472.
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O'Brien JE, Kibiryeva N, Zhou XG, Marshall JA, Lofland GK, Artman M, Chen J, Bittel DC. Noncoding RNA expression in myocardium from infants with tetralogy of Fallot. Circ Cardiovasc Genet. 2012 Jun; 5(3):279-86.
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Bittel DC, Butler MG, Kibiryeva N, Marshall JA, Chen J, Lofland GK, O'Brien JE. Gene expression in cardiac tissues from infants with idiopathic conotruncal defects. BMC Med Genomics. 2011 Jan 05; 4:1.
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