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dc.contributor.authorFidan, Süleyman Emre
dc.contributor.authorKoçyiğit, Süleyman Emre
dc.date.accessioned2024-12-19T06:24:21Z
dc.date.available2024-12-19T06:24:21Z
dc.date.issued2024en_US
dc.identifier.issn1355-4794 / 1465-3656
dc.identifier.urihttps://doi.org/10.1080/13554794.2024.2436218
dc.identifier.urihttps://hdl.handle.net/20.500.12462/15570
dc.description.abstractColpocephaly, a cause of hydrocephalus, is characterized by disproportionately enlarged occipital horns of the lateral ventricles. It is rarely seen in the older adults. Few cases were reported as colpocephaly in elderly individuals in the literature. However, it has not been reported as idiopathic normal pressure hydrocephalus-like clinical presentation in older adults. To the best of our knowledge, the co-existence of colpocephaly and Alzheimer’s disease has not been reported previously. In these respects, it is the first case in the literature. © 2024 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.language.isoengen_US
dc.publisherRoutledge Journals, Taylor & Francıs Ltden_US
dc.relation.isversionof10.1080/13554794.2024.2436218en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectColpocephalyen_US
dc.subjectIdiopathic Normal Pressure Hydrocephalusen_US
dc.subjectDementiaen_US
dc.subjectAgingen_US
dc.subjectGeriatric Assessmenen_US
dc.titleA case of mimicking normal pressure hydrocephalus in a female older patient: Coexistence of probable Alzheimer’s dementia and colpocephalyen_US
dc.typearticleen_US
dc.relation.journalNeurocaseen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0003-2025-8263en_US
dc.identifier.volume2024en_US
dc.identifier.issueDecemberen_US
dc.identifier.startpage1en_US
dc.identifier.endpage5en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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