"Choanal 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.
A congenital abnormality that is characterized by a blocked CHOANAE, the opening between the nose and the NASOPHARYNX. Blockage can be unilateral or bilateral; bony or membranous.
| Descriptor ID |
D002754
|
| MeSH Number(s) |
C08.460.171 C08.695.271 C09.603.171 C16.131.740.271
|
| Concept/Terms |
Choanal Atresia- Choanal Atresia
- Atresia, Choanal
- Atresias, Choanal
- Choanal Atresias
|
Below are MeSH descriptors whose meaning is more general than "Choanal Atresia".
Below are MeSH descriptors whose meaning is more specific than "Choanal Atresia".
This graph shows the total number of publications written about "Choanal Atresia" by people in this website by year, and whether "Choanal Atresia" 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 |
|---|
| 2002 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 3 | 0 | 3 |
| 2016 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Choanal Atresia" by people in Profiles.
-
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. Am J Hum Genet. 2016 Feb 04; 98(2):373-81.
-
Association between thyroxine levels at birth and choanal atresia or stenosis among infants in Texas, 2004-2007. Birth Defects Res A Clin Mol Teratol. 2012 Nov; 94(11):951-4.
-
Are stents necessary after choanal atresia repair? Laryngoscope. 2012 Nov; 122(11):2365-6.
-
Maternal residential atrazine exposure and risk for choanal atresia and stenosis in offspring. J Pediatr. 2013 Mar; 162(3):581-6.
-
Balloon dilation for management of choanal atresia and stenosis. Int J Pediatr Otorhinolaryngol. 2011 Dec; 75(12):1515-8.
-
SNP genotyping to screen for a common deletion in CHARGE syndrome. BMC Med Genet. 2005 Feb 14; 6:8.
-
SEMA3E mutation in a patient with CHARGE syndrome. J Med Genet. 2004 Jul; 41(7):e94.
-
Exclusion of PITX2 mutations as a major cause of CHARGE association. Am J Med Genet. 2002 Jul 22; 111(1):27-30.
-
Airway complications in CHARGE association. Arch Otolaryngol Head Neck Surg. 1990 May; 116(5):594-5.
-
Computed tomography in the evaluation of choanal atresia in infants and children. Laryngoscope. 1987 Feb; 97(2):174-83.