Apert Syndrome: A Case Report

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dc.contributor.authorİleri, Z.
dc.contributor.authorGoyenc, Y. B.
dc.date.accessioned2020-03-26T18:32:35Z
dc.date.available2020-03-26T18:32:35Z
dc.date.issued2012
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractThe purpose of this report is to present Apert syndrome patient by highlighting craniofacial characteristics and orthodontic approach to treatment. The patient, a 16-day-old female and the second child of healthy parents, was admitted to our department with primary complaint of cleft palate. She had a cone-shaped calvarium, midface hypoplasia, syndactyly of the hands and feet, hypertelorism, proptosis and cleft palate. After taking maxillary impression, an acrylic appliance was applied to orientate the growing and enable the feeding. A case with Apert syndrome undergoes the orthodontic treatment for a long time and also a multidisciplinary approach is essential to determine the best collaborative corrective plan for the deficiencies of the patient.en_US
dc.identifier.citationİleri, Z., Goyenc, Y. B., (2012). Apert Syndrome: A Case Report. European Journal of Dentistry, 6(1), 110-113.
dc.identifier.endpage113en_US
dc.identifier.issn1305-7456en_US
dc.identifier.issue1en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage110en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/28729
dc.identifier.volume6en_US
dc.indekslendigikaynakScopusen_US
dc.institutionauthorİleri, Z.
dc.language.isoenen_US
dc.relation.ispartofEuropean Journal of Dentistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectApert Syndromeen_US
dc.subjectCraniosynostosisen_US
dc.subjectNewborn Infanten_US
dc.titleApert Syndrome: A Case Reporten_US
dc.typeArticleen_US

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