Apert's Syndrome: Ophthalmic Importance and Clinical Findings

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dc.contributor.authorCaca, Ihsan
dc.contributor.authorCaca, Fatma Nur
dc.contributor.authorSakalar, Yildirim Bayezit
dc.contributor.authorErdem, Seyfettin
dc.contributor.authorAlakus, Fuat
dc.contributor.authorCiftci, Suleyman
dc.contributor.authorDogan, Eyuep
dc.date.accessioned2024-04-24T17:44:28Z
dc.date.available2024-04-24T17:44:28Z
dc.date.issued2009
dc.departmentDicle Üniversitesien_US
dc.description.abstractApert's syndrome is a rare form of craniosynostosis that exhibits with many ocular manifestations. We present two cases of Apert's syndrome. Our first case is a 10-year-old girl admitted with exotropia, V pattern and proptosis on examination. Investigations revealed coronal craniosynostosis, cleft palate, vaginal atresia and syndactyly of the hands and feet. The second case is a 5-year-old boy presented with hypertelorism, exotropia, dissociated vertical deviation and proptosis. Investigations revealed coronal craniosynostosis, bifid uvula and syndactyly of the hands and feeten_US
dc.identifier.endpage46en_US
dc.identifier.issn1530-4086
dc.identifier.issue1en_US
dc.identifier.pmid19413227
dc.identifier.startpage44en_US
dc.identifier.urihttps://hdl.handle.net/11468/22088
dc.identifier.volume41en_US
dc.identifier.wosWOS:000265434100008
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherAmer Soc Contemporary Medicine Surgery & Ophthalmologyen_US
dc.relation.ispartofAnnals of Ophthalmology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleApert's Syndrome: Ophthalmic Importance and Clinical Findingsen_US
dc.titleApert's Syndrome: Ophthalmic Importance and Clinical Findings
dc.typeArticleen_US

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