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dc.contributor.authorBiçer, Özlem
dc.date.accessioned2020-11-20T08:09:04Z
dc.date.available2020-11-20T08:09:04Z
dc.date.issued2018
dc.identifier.urihttps://doi.org/10.4274/tjo.89166tr_TR
dc.identifier.urihttp://hdl.handle.net/20.500.12575/72490
dc.description.abstractPachychoroid neovasculopathy (PNV) is a form of type 1 neovascularization characterized by dilated choroidal vessels in areas of increased choroidal thickness. In this article, we describe a patient diagnosed with PNV. A 50-year-old male with a 2-month history of blurred vision was referred to our clinic. His best corrected visual acuity was 20/100 in both eyes. Retinal pigment epithelium alterations, which were more prominent in fundus autofluorescence, were detected in both eyes on dilated fundus examination. Characteristic findings of PNV were detected in fundus fluorescein angiography, indocyanine green angiography, spectral domain optical coherence tomography, and optical coherence tomography angiography.tr_TR
dc.language.isoentr_TR
dc.relation.isversionof10.4274/tjo.89166tr_TR
dc.subjectchoroidal neovascularizationtr_TR
dc.subjectoptical coherence tomography angiographytr_TR
dc.subjectPachychoroid neovasculopathytr_TR
dc.titleMultimodal Imaging in Pachychoroid Neovasculopathy: A Case Reporttr_TR
dc.typeArticletr_TR
dc.relation.journalTurk J Ophthalmol.tr_TR
dc.contributor.departmentTıp Fakültesitr_TR
dc.identifier.volume48tr_TR
dc.identifier.issue5tr_TR
dc.identifier.startpage262tr_TR
dc.identifier.endpage266tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıtr_TR


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