| Literature DB >> 34172206 |
Patricio Varela1, Claudia Schweiger2.
Abstract
Congenital airway anomalies (CAA) include a variety of conditions that cause respiratory distress in neonates and infants. These malformations occur at various anatomic levels and manifest in a wide spectrum of airway symptoms, with presentation significantly influenced by the level at which obstruction occurs as well as by the severity of obstruction. The prevalence of congenital airway malformations has been estimated to range between 0.2 and 1 in 10,000 live births. The most frequent CAA are laryngomalacia, bilateral vocal cord paralysis, subglottic stenosis, laryngeal webs, subglottic hemangioma, tracheomalacia, congenital tracheal stenosis, laryngotracheal cleft, and tracheal agenesis.Entities:
Keywords: Clefts; Congenital malformations; Congenital subglottic stenosis; Exit procedure; Laryngeal atresia; Tracheal stenosis; Tracheomalacia; Tracheoplasty
Year: 2021 PMID: 34172206 DOI: 10.1016/j.sempedsurg.2021.151055
Source DB: PubMed Journal: Semin Pediatr Surg ISSN: 1055-8586 Impact factor: 2.754