| dc.contributor.author | Gencay, Isin | |
| dc.date.accessioned | 2020-06-25T18:34:15Z | |
| dc.date.available | 2020-06-25T18:34:15Z | |
| dc.date.issued | 2019 | |
| dc.identifier.citation | closedAccess | en_US |
| dc.identifier.issn | 1049-2275 | |
| dc.identifier.issn | 1536-3732 | |
| dc.identifier.uri | https://doi.org/10.1097/SCS.0000000000004833 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/7836 | |
| dc.description | WOS: 000467717400080 | en_US |
| dc.description | PubMed: 31137453 | en_US |
| dc.description.abstract | Apert syndrome is one of the acrocephalosyndactilia syndromes that is characterized with calvarial an extremity deformities. Anesthesia management of this syndrome is commonly related with difficult airway. However, hyponatremia is another insistent complication that can occur during craniosynostosis surgeries. Hyponatremia is a common complication during calvarial remodeling surgeries and it can result in serious neurologic damage. Development of mild hyponatremia in a patient with Apert syndrome that went under craniosynostosis surgery was presented in this study. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Lippincott Williams & Wilkins | en_US |
| dc.relation.isversionof | 10.1097/SCS.0000000000004833 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Apert syndrome | en_US |
| dc.subject | craniosynostosis surgery | en_US |
| dc.subject | hyponatremia | en_US |
| dc.title | Apert Syndrome: Intraoperative and Postoperative Hyponatremia | en_US |
| dc.type | article | en_US |
| dc.contributor.department | Kırıkkale Üniversitesi | en_US |
| dc.identifier.volume | 30 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 508 | en_US |
| dc.identifier.endpage | 509 | en_US |
| dc.relation.journal | Journal Of Craniofacial Surgery | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
