Publication:
Retinitis pigmentosa in childhood: A case report

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dc.contributor.authorTığ, Ufuk Fiahin
dc.contributor.authorKendir, Fadime
dc.contributor.authorAyata, Ali
dc.contributor.buuauthorEren, Erdal
dc.contributor.buuauthorEREN, ERDAL
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.contributor.orcid0000-0002-1684-1053
dc.contributor.researcheridJPK-3909-2023
dc.date.accessioned2024-09-17T07:00:45Z
dc.date.available2024-09-17T07:00:45Z
dc.date.issued2008-06-01
dc.description.abstractRetinitis pigmentosa (RP) is characterized by progressive loss of vision and accompanied by many syndromes. Therefore, early diagnosis is very important in RP. Now, definitive treatment of RP is not available. Diagnosis is performed with good medical history and ophthalmolojical examination. We present a patient with RP and describe diagnosis, treatment and approach to this disease.
dc.identifier.endpage46
dc.identifier.issn1304-9054
dc.identifier.issue1
dc.identifier.startpage43
dc.identifier.urihttps://hdl.handle.net/11452/44814
dc.identifier.volume6
dc.identifier.wos000422249900009
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherGalenos Yayincilik
dc.relation.journalGuncel Pediatri-journal Of Current Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectRetinitis pigmentosa
dc.subjectChild
dc.subjectBlindness
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectPediatrics
dc.titleRetinitis pigmentosa in childhood: A case report
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
local.indexed.atWOS
relation.isAuthorOfPublication2d1c6521-88a9-4270-9918-92f16f98006c
relation.isAuthorOfPublication.latestForDiscovery2d1c6521-88a9-4270-9918-92f16f98006c

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