Persistent cerebellar syndrome due to lithium treatment: a case report

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dc.contributor.authorSahingoz, Mine
dc.contributor.authorDagistanli, Adnan Alper
dc.date.accessioned2024-02-23T14:41:32Z
dc.date.available2024-02-23T14:41:32Z
dc.date.issued2013
dc.departmentNEÜen_US
dc.description.abstractWe report the case of a 23-year-old man with bipolar disorder who developed permanent cerebellar damage of lithium intake within therapeutic ranges. Cerebellar symptoms such as dysarthria, ataxia, and tremor developed 1 year after the beginning of lithium. Two years later, cerebellar signs and symptoms were found to be permanent in the patient. Cerebellar syndrome was most probably due to lithium neurotoxicity, which was associated with the administration of antipsychotic.en_US
dc.identifier.doi10.5455/jmood.20130701042241
dc.identifier.endpage134en_US
dc.identifier.issn2146-1473
dc.identifier.issn2146-2380
dc.identifier.issue3en_US
dc.identifier.startpage131en_US
dc.identifier.urihttps://doi.org/10.5455/jmood.20130701042241
dc.identifier.urihttps://hdl.handle.net/20.500.12452/16893
dc.identifier.volume3en_US
dc.identifier.wosWOS:000421350500007en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherYerkure Tanitim & Yayincilik Hizmetleri A Sen_US
dc.relation.ispartofJournal Of Mood Disordersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectLithiumen_US
dc.subjectCerebellar Syndromeen_US
dc.subjectPermanent Neurotoxicityen_US
dc.titlePersistent cerebellar syndrome due to lithium treatment: a case reporten_US
dc.typeArticleen_US

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