Central areolar choroidal dystrophy case
| dc.authorid | 0000-0003-2445-6339 | |
| dc.authorid | 0000-0001-8893-1739 | |
| dc.authorid | 0000-0002-8851-6559 | |
| dc.contributor.author | Tanrıverdi, Cafer | |
| dc.contributor.author | Nurözler Tabakçı, Burcu | |
| dc.contributor.author | Şentürk, Fevzi | |
| dc.date.accessioned | 2020-12-21T10:26:30Z | |
| dc.date.available | 2020-12-21T10:26:30Z | |
| dc.date.issued | 2020 | |
| dc.department | İstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Göz Hastalıkları Ana Bilim Dalı | |
| dc.description.abstract | Central 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.citation | Tanrıverdi, 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.doi | 10.37845/RET.VIT.2020.29.27 | |
| dc.identifier.endpage | 156 | |
| dc.identifier.issn | 1300-1256 | |
| dc.identifier.issue | 2 | |
| dc.identifier.scopusquality | Q4 | |
| dc.identifier.startpage | 152 | |
| dc.identifier.uri | https://dx.doi.org/10.37845/RET.VIT.2020.29.27 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12511/6114 | |
| dc.identifier.volume | 29 | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.language.iso | en | |
| dc.publisher | Gazi Eye Foundation | |
| dc.relation.ispartof | Retina-Vitreus | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/embargoedAccess | |
| dc.subject | Dystrophy Case | |
| dc.subject | Central Areolar Choroidal | |
| dc.subject | Choroidal | |
| dc.title | Central areolar choroidal dystrophy case | |
| dc.type | Article |











