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dc.contributor.authorAydın, Ali Ekrem
dc.date.accessioned2021-06-22T13:16:09Z
dc.date.available2021-06-22T13:16:09Z
dc.date.issued2020en_US
dc.identifier.citationAydın, A. E. (2020). Pigmentary glaucoma treatment. Glokom Katarakt, 15(4), 201-205. https://dx.doi.org/10.37844/glauc.cat.2020.15.35en_US
dc.identifier.issn1305-9173
dc.identifier.issn2717-7157
dc.identifier.urihttps://dx.doi.org/10.37844/glauc.cat.2020.15.35
dc.identifier.urihttps://hdl.handle.net/20.500.12511/7271
dc.description.abstractPigment dispersion syndrome (PDS) is a clinical entity that is characterized with anomalous irido-zonular contact leading pigment dispersion throughout the anterior segment. Clinical presentation includes pigmented cells on the corneal endothelium, an increased pigmentation of the trabecular meshwork, and mid-periphery transillumination defects of iris. The syndrome is usually bilateral and more common in myopic individuals and young male adults. Also it can be associated with ocular hypertension or glaucoma. Pigmentary glaucoma (PG) is a kind of secondary open-angle glaucoma and is caused by occlusion of trabecular meshwork by pigmentary cells and reduction in the aqueous humor effl ux. In this review, we will discuss clinical characteristics, pathogenesis and current management of PDS and PG.en_US
dc.language.isoengen_US
dc.publisherGazi Göz Vakfıen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectPigmentary Glaucoma Treatmenten_US
dc.subjectEye Diseasesen_US
dc.titlePigmentary glaucoma treatmenten_US
dc.typeeditorialen_US
dc.relation.ispartofGlokom Katarakten_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Göz Hastalıkları Ana Bilim Dalıen_US
dc.identifier.volume15en_US
dc.identifier.issue4en_US
dc.identifier.startpage201en_US
dc.identifier.endpage205en_US
dc.relation.publicationcategoryDiğeren_US
dc.identifier.doi10.37844/glauc.cat.2020.15.35en_US


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