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- W2022122986 abstract "The Kluver-Bucy syndrome (KBS) is a rare cerebral neurological disorder, characterized by the symptoms of increased appetite, hypersexuality, hypermetamorphosis (strong tendency to react to visual stimulus), memory disorders, visual agnosia, dullness, aphasia, bulimia, polyuria, and polydipsia. It was first described by Kluver and Bucy in 1939. The disorder is a neuro-behavior syndrome that occurs due to the extirpation of a large section of the rhinencephalon and both temporal lobes in Rhesus monkeys. In 1955, Terzian and Ore reported the first case of KBS that developed after bilateral temporal lobectomy, which was performed for epilepsy, in a human being ( 1 Terzian H. Ore G.D. Syndrome of Kluver and Bucy; reproduced in man by bilateral removal of the temporal lobes. Neurology. 1955; 5 (cited in ref. 2): 373-380 Crossref PubMed Google Scholar ). The syndrome may be seen during the course of miscellaneous cerebrovascular events such as cerebral trauma and hypoxia, mesial temporal lobe dysfunction or destruction, and during the course of various neurological diseases such as temporal lobe epilepsy and encephalitis ( 2 Pradhan S. Singh M.N. Pandey N. et al. Kluver-Bucy syndrome in young children. Clin Neurol Neurosurg. 1998; 100: 254-258 Abstract Full Text Full Text PDF PubMed Scopus (42) Google Scholar , 3 Bono S. Raschilas F. Mari I. et al. Kluver-Bucy syndrome in herpetic meningoencephalitis [French]. Presse Med. 2001; 30: 115-118 PubMed Google Scholar ). The syndrome can occur in two forms, complete and incomplete forms. Herein, we report an 8-year-old boy diagnosed with incomplete KBS during acute encephalitis." @default.
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- W2022122986 date "2008-08-01" @default.
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- W2022122986 title "A Child with Incomplete Kluver-Bucy Syndrome Developed During Acute Encephalitis" @default.
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- W2022122986 doi "https://doi.org/10.1016/j.jemermed.2007.05.051" @default.
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