"Heart Septal Defects" 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.
Abnormalities in any part of the HEART SEPTUM resulting in abnormal communication between the left and the right chambers of the heart. The abnormal blood flow inside the heart may be caused by defects in the ATRIAL SEPTUM, the VENTRICULAR SEPTUM, or both.
| Descriptor ID |
D006343
|
| MeSH Number(s) |
C14.240.400.560 C14.280.400.560 C16.131.240.400.560
|
| Concept/Terms |
Heart Septal Defects- Heart Septal Defects
- Defect, Heart Septal
- Defects, Heart Septal
- Heart Septal Defect
- Septal Defect, Heart
- Septal Defects, Heart
- Cardiac Septal Defects
|
Below are MeSH descriptors whose meaning is more general than "Heart Septal Defects".
Below are MeSH descriptors whose meaning is more specific than "Heart Septal Defects".
This graph shows the total number of publications written about "Heart Septal Defects" by people in this website by year, and whether "Heart Septal Defects" 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 |
|---|
| 2003 | 0 | 2 | 2 |
| 2006 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 3 | 0 | 3 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Heart Septal Defects" by people in Profiles.
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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Sci Rep. 2020 10 22; 10(1):18051.
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Percutaneous closure of an acquired Gerbode defect. Eur Heart J Cardiovasc Imaging. 2016 Dec; 17(12):1439.
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Shunt Lesions Part I: Patent Ductus Arteriosus, Atrial Septal Defect, Ventricular Septal Defect, and Atrioventricular Septal Defect. Pediatr Crit Care Med. 2016 08; 17(8 Suppl 1):S302-9.
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Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 07 15; 25(14):3011-3028.
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De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS Genet. 2016 Apr; 12(4):e1005963.
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Long-term outcomes after surgical repair of complete atrioventricular septal defect. J Thorac Cardiovasc Surg. 2015 Aug; 150(2):369-74.
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Modified single patch: are we still worried about subaortic stenosis? Ann Thorac Surg. 2015 May; 99(5):1671-5; discussion 1675-6.
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Foxf genes integrate tbx5 and hedgehog pathways in the second heart field for cardiac septation. PLoS Genet. 2014 Oct; 10(10):e1004604.
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Invited commentary. Ann Thorac Surg. 2014 Feb; 97(2):671-2.
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Atrial tachyarrhythmias and the Cox-maze procedure in congenital heart disease. Congenit Heart Dis. 2013 Sep-Oct; 8(5):434-9.