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Article: Mah-jong - Induced seizures: Case reports and review of twenty-three patients

TitleMah-jong - Induced seizures: Case reports and review of twenty-three patients
Authors
KeywordsCerebral cortex
Electroencephalography
Epilepsy, generalized
Epilepsy, reflex
Gambling
Issue Date2007
PublisherHong Kong Medical Association. The Journal's web site is located at http://www.hkmj.org/resources/supp.html
Citation
Hong Kong Medical Journal, 2007, v. 13 n. 4, p. 314-318 How to Cite?
Abstract'Mah-jong epilepsy' is a rare reflex epilepsy syndrome, manifesting as recurrent epileptic seizures triggered by either playing or just watching mah-jong. We present three patients with this condition and review all the reported cases. Mah-jong - induced seizures can be considered a subtype of cognition-induced epilepsy. Nonetheless, these patients have distinctive clinical and electrophysiological features: late age of onset, different seizure patterns, single seizure-trigger, lack of spontaneous seizures, and electroencephalographic findings not supportive of idiopathic generalised epilepsy. The pathophysiological mechanism underlying mah-jong - induced seizures may be different from the other cognition-associated reflex epileptic phenomena.
Persistent Identifierhttp://hdl.handle.net/10722/163101
ISSN
2021 Impact Factor: 1.256
2020 SCImago Journal Rankings: 0.357
References

 

DC FieldValueLanguage
dc.contributor.authorChang, RSKen_US
dc.contributor.authorCheung, RTFen_US
dc.contributor.authorHo, SLen_US
dc.contributor.authorMak, Wen_US
dc.date.accessioned2012-09-05T05:27:36Z-
dc.date.available2012-09-05T05:27:36Z-
dc.date.issued2007en_US
dc.identifier.citationHong Kong Medical Journal, 2007, v. 13 n. 4, p. 314-318en_US
dc.identifier.issn1024-2708en_US
dc.identifier.urihttp://hdl.handle.net/10722/163101-
dc.description.abstract'Mah-jong epilepsy' is a rare reflex epilepsy syndrome, manifesting as recurrent epileptic seizures triggered by either playing or just watching mah-jong. We present three patients with this condition and review all the reported cases. Mah-jong - induced seizures can be considered a subtype of cognition-induced epilepsy. Nonetheless, these patients have distinctive clinical and electrophysiological features: late age of onset, different seizure patterns, single seizure-trigger, lack of spontaneous seizures, and electroencephalographic findings not supportive of idiopathic generalised epilepsy. The pathophysiological mechanism underlying mah-jong - induced seizures may be different from the other cognition-associated reflex epileptic phenomena.en_US
dc.languageengen_US
dc.publisherHong Kong Medical Association. The Journal's web site is located at http://www.hkmj.org/resources/supp.htmlen_US
dc.relation.ispartofHong Kong Medical Journalen_US
dc.rightsHong Kong Medical Journal. Copyright © Hong Kong Medical Association.-
dc.subjectCerebral cortex-
dc.subjectElectroencephalography-
dc.subjectEpilepsy, generalized-
dc.subjectEpilepsy, reflex-
dc.subjectGambling-
dc.subject.meshAdulten_US
dc.subject.meshEpilepsy, Reflex - Etiologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshRecreationen_US
dc.titleMah-jong - Induced seizures: Case reports and review of twenty-three patientsen_US
dc.typeArticleen_US
dc.identifier.emailCheung, RTF:rtcheung@hku.hken_US
dc.identifier.emailHo, SL:slho@hku.hken_US
dc.identifier.authorityCheung, RTF=rp00434en_US
dc.identifier.authorityHo, SL=rp00240en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid17664536-
dc.identifier.scopuseid_2-s2.0-34548214637en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-34548214637&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume13en_US
dc.identifier.issue4en_US
dc.identifier.spage314en_US
dc.identifier.epage318en_US
dc.publisher.placeHong Kongen_US
dc.identifier.scopusauthoridChang, RSK=36725285000en_US
dc.identifier.scopusauthoridCheung, RTF=7202397498en_US
dc.identifier.scopusauthoridHo, SL=25959633500en_US
dc.identifier.scopusauthoridMak, W=22948344000en_US
dc.identifier.issnl1024-2708-

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