Literature DB >> 1067145

Bilateral congenital choanal atresia and absence of respiratory distress.

N Beligere, D Caldarelli, S Pruzansky.   

Abstract

Bilateral congenital choanal atresia is considered a lethal congenital malformation in an obligatory nasal breathing neonate. Described herein are two cases of bilateral choanal atresia associated with craniofacial anomalies who did not present respiratory distress in the neonatal period. Our first patient had a complete unilateral cleft lip which facilitated oropharyngeal respiration. The second patient presented wory distress in the neonatal period by providing an oropharyngeal airway.

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Year:  1976        PMID: 1067145

Source DB:  PubMed          Journal:  Cleft Palate J        ISSN: 0009-8701


  2 in total

1.  Congenital anomalies in patients with choanal atresia: CHARGE-association.

Authors:  B Koletzko; F Majewski
Journal:  Eur J Pediatr       Date:  1984-09       Impact factor: 3.183

2.  Airway management in neonate with Microcuff(®) Pediatric endotracheal tube for correction of bilateral choanal atresia.

Authors:  Tuhin Mistry; Neelam Dogra; Priyanka Jain; Kanchan Chauhan
Journal:  Anesth Essays Res       Date:  2016 Jan-Apr
  2 in total

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