Central areolar choroidal dystrophy case

dc.authorid0000-0003-2445-6339
dc.authorid0000-0001-8893-1739
dc.authorid0000-0002-8851-6559
dc.contributor.authorTanrıverdi, Cafer
dc.contributor.authorNurözler Tabakçı, Burcu
dc.contributor.authorŞentürk, Fevzi
dc.date.accessioned2020-12-21T10:26:30Z
dc.date.available2020-12-21T10:26:30Z
dc.date.issued2020
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Göz Hastalıkları Ana Bilim Dalı
dc.description.abstractCentral areolar choroidal dystrophy is a rarely seen, hereditary retinal disease which primarily affects macula. Here, we aimed to review clinical findings, ophthalmological imaging results and electrodiagnostic test results in a 43-years old man presented with visual impairment to our clinic and diagnosed as central areolar choroidal dystrophy.
dc.identifier.citationTanrıverdi, C., Nurözler Tabakçı, B. ve Şentürk, F. (2020). Central areolar choroidal dystrophy case. Retina-Vitreus, 29(2), 152-156. https://dx.doi.org/10.37845/RET.VIT.2020.29.27
dc.identifier.doi10.37845/RET.VIT.2020.29.27
dc.identifier.endpage156
dc.identifier.issn1300-1256
dc.identifier.issue2
dc.identifier.scopusqualityQ4
dc.identifier.startpage152
dc.identifier.urihttps://dx.doi.org/10.37845/RET.VIT.2020.29.27
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6114
dc.identifier.volume29
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.publisherGazi Eye Foundation
dc.relation.ispartofRetina-Vitreusen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/embargoedAccess
dc.subjectDystrophy Case
dc.subjectCentral Areolar Choroidal
dc.subjectChoroidal
dc.titleCentral areolar choroidal dystrophy case
dc.typeArticle

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