Optic disc drusen mimicking papilledema in an infant with Joubert syndrome

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dc.contributor.authorYilmaz S.
dc.contributor.authorDemirkilinc Biler E.
dc.contributor.authorEce Solmaz A.
dc.contributor.authorSerdaroglu G.
dc.contributor.authorGazeteci Tekin H.
dc.contributor.authorGokben S.
dc.date.accessioned2019-10-26T21:23:06Z
dc.date.available2019-10-26T21:23:06Z
dc.date.issued2015
dc.departmentEge Üniversitesien_US
dc.description.abstractOptic disc drusen mimicking papilledema in an infant with Joubert syndrome: Joubert Syndrome is a rare autosomal recessive disorder characterized by absence or underdevelopment of the cerebellar vermis. Various ocular and oculomotor findings are frequently seen in cases with Joubert Syndrome. However, only three adolescent patients with Joubert Syndrome were diagnosed with optic disc drusen. Here we present an infant case of Joubert Syndrome referred with papilledema and diagnosed with optic disc drusen.en_US
dc.identifier.endpage39en_US
dc.identifier.issn1015-8146
dc.identifier.issue1en_US
dc.identifier.pmid26043505en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage35en_US
dc.identifier.urihttps://hdl.handle.net/11454/17034
dc.identifier.volume26en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherEditions Medecine et Hygieneen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectInfanten_US
dc.subjectJoubert syndromeen_US
dc.subjectOptic disc drusenen_US
dc.subjectPseudopapilledemaen_US
dc.titleOptic disc drusen mimicking papilledema in an infant with Joubert syndromeen_US
dc.typeArticleen_US

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