Document Type
Article
Department
Otolaryngology, Head and Neck Surgery; Centre for Innovation in Medical Education
Abstract
Abstract: Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with nasopharynx. Surgical repair is recommended in the first weeks of life in bilateral cases because this is a life-threatening situation in newborns. This is a case report of a full term, healthy newborn baby presenting with intermittent attacks of cyanosis and respiratory distress soon after birth. On examination, alternating cyanosis and normal colour was observed in the infant. The insertion of nasal catheters in both the nares revealed the diagnosis of bilateral CCA. For this rare condition, conservative management was followed with elective transnasal endoscopic repair to relieve the life threatening nasal obstruction at the tenth day of life.
Publication (Name of Journal)
Journal of the Pakistan Medical Association
Recommended Citation
Saleem, A. F.,
Arif, S.,
Aslam, N.,
Ikram, M.
(2010). Congenital Bilateral Choanal Atresia. Journal of the Pakistan Medical Association, 60(10), 869-72.
Available at:
https://ecommons.aku.edu/pakistan_fhs_mc_surg_otolaryngol_head_neck/52