
Anesthesia management in a patient of Apert syndrome
Author(s) -
Kiran Patel,
Dilip Chavan,
Pradnya Sawant
Publication year - 2013
Publication title -
al-banǧ. maqālāt wa abḥāṯ fī al-taẖdīr wa-al-in’āš
Language(s) - English
Resource type - Journals
ISSN - 0259-1162
DOI - 10.4103/0259-1162.114021
Subject(s) - apert syndrome , syndactyly , craniosynostosis , medicine , craniofacial , hypoplasia , dysostosis , airway management , orthopedic surgery , anesthesia , surgery , airway , congenital disease , psychiatry
Apert syndrome is autosomal dominant disease associated with multiple craniofacial and limb deformities. These children usually face many orthopedic, orthodental operative procedures. As anesthetist, we face difficulties in airway management due to mid-facial hypoplasia, craniosynostosis. We report a case of Apert syndrome which was referred to us for syndactyly release, focusing on the difficulties and complications related to it.