Sturge-Weber syndrome without facial nevus

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dc.contributor.authorGuler, Ibrahim
dc.contributor.authorKucukapan, Ahmet
dc.contributor.authorKiresi, Demet
dc.date.accessioned2024-02-23T14:34:44Z
dc.date.available2024-02-23T14:34:44Z
dc.date.issued2013
dc.departmentNEÜen_US
dc.description.abstractSturge-Weber syndrome is a rare neurocutaneous disorder. Coexistence of facial nevus with epilepsy often suggests the diagnosis of Sturge-Weber syndrome. However, the diagnosis becomes more difficult when there is no facial nevus. Radiologic examinations are often used for diagnosis and management. Especially in cases without skin findings, the radiological examinations with typical findings become more important. In this paper, we report case of a 12-year-old girl who was followed with the diagnosis of epilepsy since the age of two years, had complaints of weakness of the left arm and left leg without skin findings, and was diagnosed with Sturge-Weber syndrome after radiological examinations.en_US
dc.identifier.doi10.3233/JPN-120587
dc.identifier.endpage54en_US
dc.identifier.issn1304-2580
dc.identifier.issn1875-9041
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84874475161en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage51en_US
dc.identifier.urihttps://doi.org/10.3233/JPN-120587
dc.identifier.urihttps://hdl.handle.net/20.500.12452/15734
dc.identifier.volume11en_US
dc.identifier.wosWOS:000216256400009en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlag Kgen_US
dc.relation.ispartofJournal Of Pediatric Neurologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSturge-Weber Syndromeen_US
dc.subjectImagingen_US
dc.subjectFacial Nevusen_US
dc.titleSturge-Weber syndrome without facial nevusen_US
dc.typeArticleen_US

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