A Case of Sporadic Creutzfeldt-Jakob Disease That Developed With Psychiatric Symptoms

dc.contributor.authorOzkan, Adile
dc.contributor.authorAydin Canturk, Ilknur
dc.contributor.authorCandan, Fatma
dc.contributor.authorIsik, Nihal
dc.contributor.authorOzisik Karaman, Handan Isin
dc.date.accessioned2025-01-27T20:24:55Z
dc.date.available2025-01-27T20:24:55Z
dc.date.issued2015
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractCreutzfeldt-Jakob disease (CJD) is a fairly rare prion sickness characterized by rapidly progressive dementia and neuropsychiatric symptoms. The diversity of clinical characteristics of the disease causes difficulties during diagnosis. The first finding of the disease might be psychiatric symptoms. The male patient who was diagnosed with CJD after dementia, ataxia, and myoclonus developed rapidly following psychiatric symptoms, was presented in order to draw attention to the onset with psychiatric symptoms in CJD.
dc.identifier.endpage216
dc.identifier.issn1300-2163
dc.identifier.issue3
dc.identifier.pmid26364176
dc.identifier.startpage213
dc.identifier.urihttps://hdl.handle.net/20.500.12428/22386
dc.identifier.volume26
dc.identifier.wosWOS:000360779500009
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isotr
dc.publisherTurkiye Sinir Ve Ruh Sagligi Dernegi
dc.relation.ispartofTurk Psikiyatri Dergisi
dc.relation.publicationcategoryinfo:eu-repo/semantics/openAccess
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20250125
dc.subjectCreutzfeldt-Jakob disease
dc.subjectpsychiatry
dc.subjectdementia
dc.titleA Case of Sporadic Creutzfeldt-Jakob Disease That Developed With Psychiatric Symptoms
dc.typeArticle

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