VIII: Congenital laryngeal cleft

J. E. Delahunty, Jerrie Cherry

Research output: Contribution to journalArticlepeer-review

Abstract

Congenital laryngeal cleft is a rare anomaly. It is suggested, however, that the limited number of cases to be found in the literature may, in part, result from a failure to identify the lesion. The clinical picture is characteristically that of a newborn with respiratory difficulties associated with feeding, and excess mucus. The differential diagnosis consists primarily of tracheo-esophageal fistula and bilateral choanal atresia. The cleft may involve the cricoid cartilage without extending into the tracheo-esophageal septum and the difficulties associated with establishing the diagnosis in such cases are stressed. The treatment is surgical, and the fourth case so far reported in the literature to have undergone successful surgery is included in this series of congenital laryngeal clefts.

Original languageEnglish (US)
Pages (from-to)96-106
Number of pages11
JournalAnnals of Otology, Rhinology & Laryngology
Volume78
Issue number1
DOIs
StatePublished - Feb 1969

ASJC Scopus subject areas

  • Otorhinolaryngology

Fingerprint Dive into the research topics of 'VIII: Congenital laryngeal cleft'. Together they form a unique fingerprint.

Cite this