Anesthesia challenges in a case of Crouzon syndrome for corrective rigid external distraction frame insertion
Crouzon syndrome is an autosomal dominant disease occurs in approximately 1 in 25,000 births, due to a mutation in the fibroblast growth factor receptor 2 gene on chromosome 10 characterized by craniosynostosis, mid-face hypoplasia, hypertelorism, high-arched palate, skull base abnormalities, and ex...
Main Authors: | Veena Ganeriwal, Paulomi Dey, Baburao Gore, Tejesh Hujare |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2019-01-01
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Series: | The Indian Anaesthetists' Forum |
Subjects: | |
Online Access: | http://www.theiaforum.org/article.asp?issn=2589-7934;year=2019;volume=20;issue=1;spage=42;epage=45;aulast=Ganeriwal |
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