Lenz microphthalmia syndrome with dental anomalies: A case report

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dc.contributor.authorErsin N.K.
dc.contributor.authorTugsel Z.
dc.contributor.authorGökce B.
dc.contributor.authorOzpinar B.
dc.contributor.authorEronat N.
dc.date.accessioned2019-10-27T00:23:21Z
dc.date.available2019-10-27T00:23:21Z
dc.date.issued2003
dc.departmentEge Üniversitesien_US
dc.description.abstractThis report describes the dental management and 7-year follow-up of a 14-year-old boy who showed the typical characteristics of Lenz microphthalmia syndrome, a rare genetic disorder characterized by multiple abnormalities. The main features of the syndrome are microphthalmia, developmental retardation, ear abnormalities, microcephaly, skeletal, digital and urogenital anomalies. The dental anomalies include micrognathia, hypodontia, agenesis of permanent teeth, conic-shaped incisors, and taurodontic molars. The purpose of the report was to document specific oral manifestations and dental anomalies and their management associated with a previously reported case.en_US
dc.identifier.endpage265en_US
dc.identifier.issn1551-8949
dc.identifier.issue3en_US
dc.identifier.pmid14998213en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage262en_US
dc.identifier.urihttps://hdl.handle.net/11454/22795
dc.identifier.volume70en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Dentistry for Childrenen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDental anomaliesen_US
dc.subjectLenz microphthalmiaen_US
dc.titleLenz microphthalmia syndrome with dental anomalies: A case reporten_US
dc.typeArticleen_US

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