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
Main Authors: Gamze Küçükosman, Bengü Gülhan Aydın, Bahar Aktaş, Hilal Ayoğlu
Format: Article
Language:English
Published: Galenos Yayinevi 2018-06-01
Series:Haseki Tıp Bülteni
Subjects:
Online Access:http://www.hasekidergisi.com/archives/archive-detail/article-preview/anesthetic-management-of-patient-for-case-with-ape/19012