Variant case of sturge-weber syndrome

dc.contributor.authorEliaçık, Sinan
dc.date.accessioned2019-05-13T09:08:29Z
dc.date.available2019-05-13T09:08:29Z
dc.date.issued2018
dc.departmentHitit Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü
dc.description.abstractDear Editor, A 17-year-old male was admitted to hospital with epileptic seizures. It was learnt that he had seizures since he was aged one year. He had no febrile seizures and his neuromotor development was normal. In his seizures, which lasted less than one minute, his eyes and head deviated to the right and sometimes licking and mouth automatisms were added. It was learnt that his number of seizures sometimes increased and seizures evolved to secondary generalized seizures. It was learnt from his family that he had not used valproic acid regularly for the last one year and he could not receive regular examinations because of socio-economic reasons.
dc.identifier.citationEliaçık, S. (2018). Variant case of sturge-weber syndrome. Türk Nöroloji Dergisi, 24(1), 72-73.
dc.identifier.doi10.4274/tnd.67674
dc.identifier.endpage73en_US
dc.identifier.issn1301-062X
dc.identifier.issue1en_US
dc.identifier.scopusqualityQ4
dc.identifier.startpage72en_US
dc.identifier.urihttps://doi.org/10.4274/tnd.67674
dc.identifier.urihttps://hdl.handle.net/11491/2004
dc.identifier.volume24en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.publisherTürk Nöroloji Derneği
dc.relation.ispartofTürk Nöroloji Dergisi
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSturge-Weberen_US
dc.subjectEpilepsyen_US
dc.subjectFacial Nevusen_US
dc.subjectEpilepsien_US
dc.subjectFasiyal Nevüsen_US
dc.titleVariant case of sturge-weber syndrome
dc.title.alternativeVaryant bir sturge-weber olgusuen_US
dc.typeOther

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