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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Galenos Yayinevi
2018-06-01
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doaj-cd729ba180b44b4ca47c0da9932012212020-11-25T03:59:16ZengGalenos YayineviHaseki Tıp Bülteni1302-00722147-26882018-06-0156216216410.4274/haseki.96967Anesthetic Management of Patient for Case with Apert SyndromeGamze Küçükosman0Bengü Gülhan Aydın1Bahar Aktaş2Hilal Ayoğlu3Bülent Ecevit University Faculty of Medicine, Department of Anesthesiology and Reanimation, Zonguldak, TurkeyBülent Ecevit University Faculty of Medicine, Department of Anesthesiology and Reanimation, Zonguldak, TurkeyBülent Ecevit University Faculty of Medicine, Department of Anesthesiology and Reanimation, Zonguldak, TurkeyBülent Ecevit University Faculty of Medicine, Department of Anesthesiology and Reanimation, Zonguldak, TurkeyApert 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.http://www.hasekidergisi.com/archives/archive-detail/article-preview/anesthetic-management-of-patient-for-case-with-ape/19012AnesthesiaApert syndromeextremities-craniofacial abnormalities |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Gamze Küçükosman Bengü Gülhan Aydın Bahar Aktaş Hilal Ayoğlu |
spellingShingle |
Gamze Küçükosman Bengü Gülhan Aydın Bahar Aktaş Hilal Ayoğlu Anesthetic Management of Patient for Case with Apert Syndrome Haseki Tıp Bülteni Anesthesia Apert syndrome extremities-craniofacial abnormalities |
author_facet |
Gamze Küçükosman Bengü Gülhan Aydın Bahar Aktaş Hilal Ayoğlu |
author_sort |
Gamze Küçükosman |
title |
Anesthetic Management of Patient for Case with Apert Syndrome |
title_short |
Anesthetic Management of Patient for Case with Apert Syndrome |
title_full |
Anesthetic Management of Patient for Case with Apert Syndrome |
title_fullStr |
Anesthetic Management of Patient for Case with Apert Syndrome |
title_full_unstemmed |
Anesthetic Management of Patient for Case with Apert Syndrome |
title_sort |
anesthetic management of patient for case with apert syndrome |
publisher |
Galenos Yayinevi |
series |
Haseki Tıp Bülteni |
issn |
1302-0072 2147-2688 |
publishDate |
2018-06-01 |
description |
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. |
topic |
Anesthesia Apert syndrome extremities-craniofacial abnormalities |
url |
http://www.hasekidergisi.com/archives/archive-detail/article-preview/anesthetic-management-of-patient-for-case-with-ape/19012 |
work_keys_str_mv |
AT gamzekucukosman anestheticmanagementofpatientforcasewithapertsyndrome AT bengugulhanaydın anestheticmanagementofpatientforcasewithapertsyndrome AT baharaktas anestheticmanagementofpatientforcasewithapertsyndrome AT hilalayoglu anestheticmanagementofpatientforcasewithapertsyndrome |
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1724454865602609152 |