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.
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Authors | Allen S Ho, Pedram Aleshi, Sheila E Cohen, Peter J Koltai, Alan G Cheng |
Journal | International journal of pediatric otorhinolaryngology
(Int J Pediatr Otorhinolaryngol)
Vol. 72
Issue 12
Pg. 1885-8
(Dec 2008)
ISSN: 0165-5876 [Print] Ireland |
PMID | 18947886
(Publication Type: Case Reports, Journal Article)
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Topics |
- Adult
- Female
- Humans
- Infant, Newborn
- Mandibulofacial Dysostosis
(complications)
- Respiratory Distress Syndrome, Newborn
(etiology, therapy)
- Syndrome
- Tracheotomy
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