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Kleine–Levin syndrome: a series of case reports

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dc.contributor.author Ramdurg, Santosh
dc.date.accessioned 2013-02-11T06:19:30Z
dc.date.available 2013-02-11T06:19:30Z
dc.date.issued 2012
dc.identifier.citation Sleep and Biological Rhythms. 2012; 10: 244–246. en_US
dc.identifier.issn 1479-8425
dc.identifier.uri http://hdl.handle.net/123456789/353
dc.description.abstract Kleine–Levin syndrome (KLS) is an intriguing, severe, homogenous disease, with well defined clinical features, but no clear cause or treatment. Therefore studies on KLS were done exclusively with case report or series. There are limited systemic study comparing KLS with controls on phenomenology, cause, investigations and management. We report four cases of KLS presented to us along with core symptoms, hypomanic and catatonic features. Response to treatment also different with one case responded to lithium while others required combination of therapy. KLS is still evolving disorder having cluster of varying symptoms and response to treatment. This needs further exploration and higher studies en_US
dc.language.iso en en_US
dc.publisher Wiley Publications en_US
dc.subject Hyper-sexuality en_US
dc.subject Hypersomnia en_US
dc.subject Kleine-levin syndrome en_US
dc.title Kleine–Levin syndrome: a series of case reports en_US
dc.type Article en_US


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