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Apert Syndrome: A Case Report and Review of the Literature

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dc.authorscopusid18036882700
dc.authorscopusid55923807300
dc.authorscopusid6602274084
dc.authorscopusid7004140928
dc.authorscopusid7003539720
dc.contributor.authorAçıkgöz, Y.
dc.contributor.authorBelet, Nursen
dc.contributor.authorYalin, T.
dc.contributor.authorIncesu, L.
dc.contributor.authorKüçüködük, Ş.
dc.date.accessioned2025-12-10T21:07:55Z
dc.date.issued2006
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Açıkgöz] Yonca, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Belet] Nurşen M., Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yalin] Türkay C., Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Incesu] Lütfi, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Küçüködük] Şükrü, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractThe prevalence of Apert syndrome is approximately 15.5 in bir million births. The principal features are craniosynostosis, midfacial hypoplasia, syndactyly of the hands and feet with mild, moderate or severe mental retardation. Inheritance is usually autosomal dominant. However most cases represent new mutations. Prenatal diagnosis has been mainly based on sonographic documentation of craniosynostosis and syndactly. A newborn with Apert syndrome is presented and related literature was reviewed in this paper.en_US
dc.identifier.endpage64en_US
dc.identifier.issn1300-2996
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-58149168569
dc.identifier.scopusqualityN/A
dc.identifier.startpage59en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34509
dc.identifier.volume23en_US
dc.identifier.wosqualityN/A
dc.language.isotren_US
dc.relation.ispartofOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApert Syndromeen_US
dc.subjectCraniosynostosisen_US
dc.subjectNewbornen_US
dc.subjectSyndactylyen_US
dc.titleApert Syndrome: A Case Report and Review of the Literatureen_US
dc.title.alternativeApert Sendromu: Olgu Sunumu ve Literatürün Gözden Geçirilmesien_US
dc.typeArticleen_US
dspace.entity.typePublication

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