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dc.contributor.authorAyvaz A.
dc.contributor.authorAtalar M.
dc.contributor.authorKoçak O.
dc.contributor.authorDilara Iça?asio?lu F.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:32:01Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:32:01Z
dc.date.issued2014
dc.identifier.issn1309-0720
dc.identifier.urihttps://dx.doi.org/10.4328/JCAM.833
dc.identifier.urihttps://hdl.handle.net/20.500.12418/5428
dc.descriptionJournal of Clinical and Analytical Medicineen_US
dc.description.abstractWalker-Warburg syndrome (WWS), a rare form of congenital muscular dystrophy, is an autosomal recessive disorder affecting the brain, eye, and muscles. In this study, three WWS cases followed in the pediatric clinic of Cumhuriyet University are presented. According to our knowledge, one of our patients is the longest-lived case who has been reported.en_US
dc.description.sponsorshipAyvaz, A.; Cumhuriyet Üniversitesi, 58040 Sivas, Turkey; email: ayvaz@ttmail.comen_US
dc.language.isoengen_US
dc.relation.isversionof10.4328/JCAM.833en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCongenital muscular dystrophybuen_US
dc.subjectDandy walker malformationen_US
dc.subjectWalker Warburg Syndrome (WWS)en_US
dc.titleThree cases of walker warburg syndrome [Walker warburg sendromlu üç Olgu]en_US
dc.typearticleen_US
dc.relation.journalJournal of Clinical and Analytical Medicineen_US
dc.contributor.departmentAyvaz, A., Pediatrik Nöroloji BD, Cumhuriyet Üniversitesi, Turkey -- Atalar, M., Radyoloji AD, Cumhuriyet Üniversitesi, Turkey -- Koçak, O., Çocuk Sa?li?i ve Hastaliklari AD, Cumhuriyet Üniversitesi, Sivas, Turkey -- Dilara Iça?asio?lu, F., Pediatrik Nöroloji BD, Cumhuriyet Üniversitesi, Turkeyen_US
dc.identifier.volume5en_US
dc.identifier.issue4en_US
dc.identifier.endpage340en_US
dc.identifier.startpage338en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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