Anesthetic Management of Patient for Case with Apert Syndrome

Apert syndrome is an autosomal dominant inherited mandibulofacial dysostosis characterized by craniosynostosis, syndactyly, high forehead, broad nose, maxillary hypoplasia, synostosis of cervical vertebrae, organ malformations, and mental retardation. It is rarely encountered and as there is little...

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Bibliographic Details
Published inHaseki tıp bülteni Vol. 56; no. 2; pp. 162 - 164
Main Authors Küçükosman, Gamze, Aydın, Bengü Gülhan, Aktaş, Bahar, Ayoğlu, Hilal
Format Journal Article
LanguageEnglish
Published Istanbul Haseki Eğitim ve Araştırma Hastanesi 01.06.2018
Galenos Publishing House
Galenos Yayinevi
Subjects
Anesthesia
Apert syndrome
Body temperature
Esophagus
extremities-craniofacial abnormalities
Intubation
Ostomy
Pediatrics
Sağlık Hizmetleri
Sleep apnea
Surgery
Tıp
Vertebrae
İstanbul
Türkiye
ekstremiteler-kafa yüz anormallikleri
Anesthesia
Apert syndrome
extremities-craniofacial abnormalities
Apert sendromu
Anestezi
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Summary:Apert syndrome is an autosomal dominant inherited mandibulofacial dysostosis characterized by craniosynostosis, syndactyly, high forehead, broad nose, maxillary hypoplasia, synostosis of cervical vertebrae, organ malformations, and mental retardation. It is rarely encountered and as there is little knowledge of the anesthesia practice for this syndrome in the literature, we present our anesthesia experience of a case undergoing bilateral syndactyly surgery.
ISSN:1302-0072
2147-2688
DOI:10.4274/haseki.96967