Bifid epiglottis syndrome

Erich M. Sturgis, Laurene L. Howell

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

True bifid epiglottis is an extremely rare laryngeal anomaly, which usually presents in the neonate with symptoms of aspiration and/or airway obstruction. Management is generally supportive observation as the symptoms lessen with age, but rarely tracheotomy is required for airway obstruction. Bifid epiglottis occurs in a syndromic picture with associated anomalies, especially polydactyly, cleft palate and retro/micrognathia but a significant number will have endocrine, gastrointestinal and genitourinary abnormalities. A case of true bifid epiglottis is presented and the literature is reviewed on the subject.

Original languageEnglish (US)
Pages (from-to)149-157
Number of pages9
JournalInternational Journal of Pediatric Otorhinolaryngology
Volume33
Issue number2
DOIs
StatePublished - Oct 1995

Keywords

  • Bifid epiglottis
  • Cleft palate
  • Congenital anomalies
  • Larynx
  • Polydactyly
  • Retrognathia

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Otorhinolaryngology

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