Endoscopic choanal atresia repair.

Congenital choanal atresia (CA) is relatively rare, with an incidence of 1 in 7,000 births with a majority being the mixed bony-membranous type. There are 5 described methods of CA repair: transpalatal, transnasal, sublabialtransnasal, transantral, and transseptal approaches. Transpalatal and transnasal have been the most popular in the last several decades with transnasal becoming the preferred technique with the advent of endoscopic instruments and techniques. In this chapter, the authors seek to describe their techniques for endoscopic transnasal repair of CA including surgical pearls for success.

[1]  M. Clementi,et al.  Treatment of hyperthyroidism in pregnancy and birth defects. , 2010, The Journal of clinical endocrinology and metabolism.

[2]  A. Fanaroff Characterization of Congenital Anomalies in Individuals With Choanal Atresia , 2009 .

[3]  H. Rodríguez,et al.  Choanal atresia associated with maternal hyperthyroidism treated with methimazole: A case–control study , 2008, American journal of medical genetics. Part A.

[4]  S. Manning,et al.  Choanal Atresia , 1996, The Laryngoscope.

[5]  G. Healy,et al.  Airway complications in CHARGE association. , 1990, Archives of otolaryngology--head & neck surgery.

[6]  R. Carpenter,et al.  Correction of congenital choanal atresia in children and adults , 1977, The Laryngoscope.