Rhombencephalosynapsis associated with dandy-walker malformation

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dc.contributor.authorSener, R. Nuri
dc.date.accessioned2019-10-27T20:01:35Z
dc.date.available2019-10-27T20:01:35Z
dc.date.issued2007
dc.departmentEge Üniversitesien_US
dc.description.abstractCoexistence of rhombencephalosynapsis and Dandy-Walker malformation has previously been documented in a fetus by autopsy. In addition, there are three cases in the imaging literature suggesting this combination. This paper reports an 8-month-old girl with clear MR imaging evidence of association of these two anomalies. The vermis was absent, and there was fusion of the cerebellar hemispheres, characteristic for rhombencephalosynapsis. The fourth ventricle showed cystic dilatation associated with an enlarged posterior fossa, characteristic for Dandy-Walker malformation. These findings suggest that rhombencephalosynapsis and Dandy-Walker malformation can coexist.en_US
dc.identifier.doi10.1111/j.1552-6569.2006.00066.xen_US
dc.identifier.endpage357en_US
dc.identifier.issn1051-2284
dc.identifier.issue4en_US
dc.identifier.pmid17894629en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage355en_US
dc.identifier.urihttps://doi.org/10.1111/j.1552-6569.2006.00066.x
dc.identifier.urihttps://hdl.handle.net/11454/41271
dc.identifier.volume17en_US
dc.identifier.wosWOS:000249827000017en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofJournal of Neuroimagingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectrhombencephalosynapsisen_US
dc.subjectDandy-Walker malformationen_US
dc.subjectposterior fossa malformationsen_US
dc.titleRhombencephalosynapsis associated with dandy-walker malformationen_US
dc.typeArticleen_US

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