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A Female Case of Kleine-Levin Syndrome Treated with Amantadine / 신경정신의학
Journal of Korean Neuropsychiatric Association ; : 725-732, 2002.
Article in Korean | WPRIM | ID: wpr-177628
ABSTRACT
Kleine-Levin syndrome is a rare disorder which usually affects adolescent males and is characterized by periodic hypersomnia, hyperphagia and abnormal behavior. This is an unexplained clinical syndrome for which several etiologies have been entertained with no standard treatment is yet available. A 18-year old woman began suffering from recurrent hypersomnia, hyperphagia, and behavioral disturbances such as irritability, derealization, and amnesia. She was normal between the episodes and diagnosed as Kleine-Levin syndrome. In the course of about two years she had 11 episodes and the mean interval between the episodes was 52.8+/-16.7 days. After application of amantadine, there were two mild episodes and then she had no episodes for more than 6 months. This case suggests the possible role of amantadine in the treatment of Kleine-Levin syndrome.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Amantadine / Hyperphagia / Kleine-Levin Syndrome / Depersonalization / Amnesia / Disorders of Excessive Somnolence Limits: Adolescent / Female / Humans / Male Language: Korean Journal: Journal of Korean Neuropsychiatric Association Year: 2002 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Amantadine / Hyperphagia / Kleine-Levin Syndrome / Depersonalization / Amnesia / Disorders of Excessive Somnolence Limits: Adolescent / Female / Humans / Male Language: Korean Journal: Journal of Korean Neuropsychiatric Association Year: 2002 Type: Article