"Esophageal Atresia" 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.
Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA.
| Descriptor ID |
D004933
|
| MeSH Number(s) |
C06.198.330 C06.405.117.260 C16.131.314.330
|
| Concept/Terms |
Esophageal Atresia- Esophageal Atresia
- Atresia, Esophageal
- Atresias, Esophageal
- Esophageal Atresias
|
Below are MeSH descriptors whose meaning is more general than "Esophageal Atresia".
Below are MeSH descriptors whose meaning is more specific than "Esophageal Atresia".
This graph shows the total number of publications written about "Esophageal Atresia" by people in this website by year, and whether "Esophageal Atresia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Esophageal Atresia" by people in Profiles.
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HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res. 2019 06 01; 111(10):591-597.
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Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula. Eur J Hum Genet. 2016 12; 24(12):1715-1723.
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Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations. Orphanet J Rare Dis. 2013 Jul 24; 8:110.
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Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother? Am J Med Genet A. 2007 Jun 01; 143A(11):1135-42.
MeSH information
