Prevalence and patterns of choanal atresia and choanal stenosis among pregnancies in Texas, 1999-2004

American Journal of Medical Genetics, Part A

Volumn 155, Issue 4, 2011, Pages 786-791

  Case, Amy P ^a   Mitchell, Laura E ^b  

^a TEXAS DEPARTMENT OF STATE HEALTH SERVICES   (United States)

^b UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

Choanal atresia; Choanal stenosis; Congenital abnormalities; Epidemiology; Prevalence; Registries

Indexed keywords

ARTICLE; BIRTH RATE; CHOANA ATRESIA; CHROMOSOME ABERRATION; CONTROLLED STUDY; DESCRIPTIVE RESEARCH; DISEASE ASSOCIATION; FEMALE; HISPANIC; HUMAN; HUMAN CELL; LIVE BIRTH; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; PATIENT CARE; PREGNANCY; PRENATAL CARE; PREVALENCE; PRIORITY JOURNAL; PROGENY; RISK FACTOR; SEX RATIO; UNITED STATES;

CALIFORNIA; CHOANAL ATRESIA; FEMALE; FRANCE; HUMANS; INHERITANCE PATTERNS; MALE; PREGNANCY; PREVALENCE; REGISTRIES; RISK FACTORS; SWEDEN; TEXAS;

EID: 79953314281     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33882     Document Type: Article

References (15)

1. Barbero P, Valdez R, Rodríguez H, Tiscornia C, Mansilla E, Allons A, Coll S, Liascovich R. 2008. Choanal atresia associated with maternal hyperthyroidism treated with methimazole: A case-control study. Am J Med Genet A 146A:2390-2395.
2. Burrow TA, Saal HM, de Alarcon A, Martin LJ, Cotton RT, Hopkin RJ. 2009. Characterization of congenital anomalies in individuals with choanal atresia. Arch Otolaryngol Head Neck Surg 135:543-547.
3. Clementi M, Di Gianantonio E, Cassina M, Leoncini E, Botto LD, Mastroiacovo P. the SAFE-Med Study Group. 2010. Treatment of hyperthyroidism in pregnancy and birth defects. J Clin Endocrinol Metab 95:E337-E341.
4. Corrales CE, Koltai PJ. 2009. Choanal atresia: Current concepts and controversies. Curr Opin Otolaryngol Head Neck Surg 17:466-470.
5. Crider KS, Cleves MA, Reefhuis J, Berry RJ, Hobbs CA, Hu DJ. 2009. Antibacterial medication use during pregnancy and risk of birth defects: National birth defects prevention study. Arch Pediatr Adolesc Med 163:978-985.
6. Dupé V, Matt N, Garnier J, Chambon P, Mark M, Ghyselinck NB. 2003. A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment. Proc Natl Acad Sci USA 100:14036-14041.
7. Foulds N, Walpole I, Elmslie F, Mansour S. 2005. Carbimazole embryopathy: An emerging phenotype. Am J Med Genet A 132A:130-135.
8. Harris J, Robert E, Källén B. 1997. Epidemiology of choanal atresia with special reference to the CHARGE association. Pediatrics 99:363-367.
9. Källén B, Mastroiacovo P, Robert E. 1996. Major congenital malformations in down syndrome. Am J Med Genet 65:160-166.
10. Kriplani A, Buckshee K, Bhargava VL, Takkar D, Ammini AC. 1994. Maternal and perinatal outcome in thyrotoxicosis complicating pregnancy. Eur J Obstet Gynecol Reprod Biol 54:159-163.
11. Kubba H, Bennett A, Bailey CM. 2004. An update on choanal atresia surgery at great ormond street hospital for children: Preliminary results with mitomycin C and the KTP laser. Int J Pediatr Otorhinolaryngol 68:939-945.
12. Pagon RA, Graham JM, Zonana J, Yong SL. 1981. Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association. J Pediatr 99:223-227.
13. Ramsden JD, Campisi P, Forte V. 2009. Choanal atresia and choanal stenosis. Otolaryngol Clin North Am 42:339-352.
14. Vissers LELM, van Ravenswaaij CMA, Admiraal R, Hurst JA, de Vries BBA, Janssen IM, van der Vliet WA, Huys EHLPG, de Jong PJ, Hamel BCJ, Schoenmakers EFPM, Brunner HG, Veltman JA, van Kessel AG. 2004. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet 36:955-957.
15. Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu Y, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC. 2004. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med 351:769-780.