Document Type
Article
Language
eng
Publication Date
1-1998
Publisher
Wiley
Source Publication
Pediatric Anesthesia
Abstract
Antley-Bixler Syndrome (ABS) is an autosomal recessive trait disorder characterized by multiple bone and cartilaginous abnormalities. Primary features include significant craniosynostosis, midface hypoplasia with choanal stenosis or atresia, femoral bowing, radiohumeral synostosis, and multiple joint contractures. Cardiac, renal, and gastrointestinal malformations have also been described. This report describes the management of a four-month-old male who underwent cranial vault remodeling to relieve craniosynostosis and discusses the potential concerns of the anaesthetist during care of children with Antley-Bixler Syndrome.
Recommended Citation
LeBard, Scott and Thiemann, Lisa, "Antley‐Bixler Syndrome: A Case Report and Discussion" (1998). College of Nursing Faculty Research and Publications. 883.
https://epublications.marquette.edu/nursing_fac/883
Comments
Accepted version. Pediatric Anesthesia, Vol. 8, No. 1 (January 1998): 89-91. DOI. © 1998 Wiley. Used with permission.