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Airway management in Nager Syndrome.

Abstract
Nager acrofacial dysostosis is a rare congenital syndrome characterized by malformed mandibulofacial structures and pre-axial upper limbs. Trismus and glossoptosis from mandibular abnormalities predisposes infants to life-threatening respiratory distress. A case of a Nager Syndrome mother delivering a similarly afflicted fetus is presented, with approaches to maintaining both tenuous airways described. Distinguishing this condition from similar syndromes is critical for care and prognosis.
AuthorsAllen S Ho, Pedram Aleshi, Sheila E Cohen, Peter J Koltai, Alan G Cheng
JournalInternational journal of pediatric otorhinolaryngology (Int J Pediatr Otorhinolaryngol) Vol. 72 Issue 12 Pg. 1885-8 (Dec 2008) ISSN: 0165-5876 [Print] Ireland
PMID18947886 (Publication Type: Case Reports, Journal Article)
Topics
  • Adult
  • Female
  • Humans
  • Infant, Newborn
  • Mandibulofacial Dysostosis (complications)
  • Respiratory Distress Syndrome, Newborn (etiology, therapy)
  • Syndrome
  • Tracheotomy

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