Kluver-Bucy syndrome developed after convulsion: A case report

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dc.authorscopusid36180210800
dc.authorscopusid8421729700
dc.authorscopusid15070346400
dc.authorscopusid35243692700
dc.authorscopusid26531350600
dc.authorscopusid7101974609
dc.contributor.authorOkur, Mesut
dc.contributor.authorYilmaz, Cahide
dc.contributor.authorEpçaçan, Serdar
dc.contributor.authorÜstyol, Lokman
dc.contributor.authorKaya, Avni
dc.contributor.authorÇaksen, Hüseyin
dc.date.accessioned2024-09-19T15:41:28Z
dc.date.available2024-09-19T15:41:28Z
dc.date.issued2011
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractKluver-Bucy syndrome is characterized by increased appetite, hypersexuality, hypermetamorphosis, memory disorders, visual agnosia, stagnancy, aphasia, bulimia, polyuria, and polydipsia. A 14 year old girl had generalized tonic-clonic convulsions at admission, and an incomplete Kluver-Bucy syndrome with hypersexuality, recent memory disturbance, hypermetamorphosis, speech disturbance, hyperactivity, agitation, aggressiveness, and hallucinations, developed the following day. Here in, we report a case of KBS in a child with epilepsy.en_US
dc.identifier.endpage217en_US
dc.identifier.issn1301-0883
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-80054096284en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage215en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/14282
dc.identifier.volume16en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofEastern Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAgitationen_US
dc.subjectChilden_US
dc.subjectEpilepsyen_US
dc.subjectHallucinationsen_US
dc.subjectHypersexualityen_US
dc.titleKluver-Bucy syndrome developed after convulsion: A case reporten_US
dc.typeArticleen_US

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