Treatment of the Patient With Crouzon Syndrome With Orthognathic Surgery

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dc.authoridsancar, bahadir/0000-0001-8804-6668
dc.authorwosidsancar, bahadir/ABH-4490-2020
dc.contributor.authorSancar, Bahadir
dc.contributor.authorTanisik, Burakhan Hakan
dc.date.accessioned2024-08-04T20:47:18Z
dc.date.available2024-08-04T20:47:18Z
dc.date.issued2020
dc.departmentİnönü Üniversitesien_US
dc.description18th International Congress of the International-Society-of-Craniofacial-Surgery (ISCFS) -- SEP 16-19, 2019 -- Paris, FRANCEen_US
dc.description.abstractCrouzon syndrome is a genetic disease that is transferred by autosomal dominant inheritance. Patients with this syndrome have craniosynostosis, hypertelorism, orbital proptosis, mid-face hypoplasia, mandibular prognathism, and concave facial profile. A number of surgical treatments are used to improve facial contours, and to correct dental and maxillary relationships. Orthognathic surgery is routinely used in the treatment of these patients. We present a female patient with Crouzon syndrome treated with Le Fort I and bilateral sagittal split osteotomy. Previously, surgically assisted rapid maxillary expansion (SARME) surgery was performed to the patient by separating the pterygomaxillary junction under general anesthesia. Down fracture was performed during the Le Fort I osteotomy without the need to separate the pterygomaxillary junction again. The facial appearance was improved with bilateral sagittal split osteotomy, and skeletal malocclusion between the jaws was treated.en_US
dc.description.sponsorshipInt Soc Craniofacial Surgen_US
dc.identifier.doi10.1097/SCS.0000000000006177
dc.identifier.endpage808en_US
dc.identifier.issn1049-2275
dc.identifier.issn1536-3732
dc.identifier.issue3en_US
dc.identifier.pmid31934979en_US
dc.identifier.scopus2-s2.0-85084961240en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage806en_US
dc.identifier.urihttps://doi.org/10.1097/SCS.0000000000006177
dc.identifier.urihttps://hdl.handle.net/11616/99292
dc.identifier.volume31en_US
dc.identifier.wosWOS:000562524800090en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofJournal of Craniofacial Surgeryen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCrouzonen_US
dc.subjectorthognathicen_US
dc.subjectSARMEen_US
dc.subjectsurgeryen_US
dc.subjectsyndromeen_US
dc.titleTreatment of the Patient With Crouzon Syndrome With Orthognathic Surgeryen_US
dc.typeConference Objecten_US

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