Konjenital herediter endotelyal distrofide göz bulguları

dc.contributor.authorÖzkağnıcı, Ahmet
dc.contributor.authorZengin, Nazmi
dc.contributor.authorGündüz, Kemal
dc.contributor.authorGültekin, Günseli
dc.contributor.authorOkudan, Süleyman
dc.date.accessioned2020-03-26T16:26:56Z
dc.date.available2020-03-26T16:26:56Z
dc.date.issued1999
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractKonjenital herediter endotelyal distrofi (KHED) nadir görülen, otozomal resesif veya otozomal dominant geçiş gösteren bir kornea hastalığıdır. Bu çalışmada KHED'li üç kardeşte (2 kız , 1 erkek) saptanan klinik bulgular sunulmuş, olgularımızda hastalığın klasik bulgularına eşlik eden alternan esotropya ve göziçi basıncı yüksekliği literatür verileri ışığında tartışılmıştır.en_US
dc.description.abstractCongenital hereditary endothelial dystrophy (CHED) is a rare corneal disorder which is inherited either as an autosomal dominant or autosomal recessive trait. In this article clinical findings in three patients from the same mother (2 sisters , 1 brother) with CHED is presented, alternating esotropia and elevated intraocular pressure accompanying the classic findings of congenital hereditary endothelial dystrophy was discussed under the light of the current literature.en_US
dc.identifier.endpage131en_US
dc.identifier.issn1300-0365en_US
dc.identifier.issn2146-9008en_US
dc.identifier.issue2en_US
dc.identifier.startpage128en_US
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/T1RVNU5qWT0=
dc.identifier.urihttps://hdl.handle.net/20.500.12395/16916
dc.identifier.volume8en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isotren_US
dc.relation.ispartofTürkiye Klinikleri Oftalmoloji Dergisien_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectGöz Hastalıklarıen_US
dc.titleKonjenital herediter endotelyal distrofide göz bulgularıen_US
dc.title.alternativeOcular fındings in congenital hereditary endothelial dystrophyen_US
dc.typeOtheren_US

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