Sturge-Weber Syndrome Type III

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dc.contributor.authorTekin, Hande Gazeteci
dc.contributor.authorGökben, Sarenur
dc.contributor.authorYılmaz, Sanem Keskin
dc.contributor.authorTekgül, Hasan
dc.contributor.authorSerdaroğlu, Gül
dc.date.accessioned2020-12-01T12:33:14Z
dc.date.available2020-12-01T12:33:14Z
dc.date.issued2018
dc.departmentEge Üniversitesien_US
dc.description.abstractSturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live births. the less common form, which can be difficult to diagnose and only involves leptomeningeal angioma, has been defined as Type III SWS. A 5.5-month-old male patient with normal neuromotor development presented with right sided partial seizures, which had been occurring frequently for the previous two days and could not be controlled. A cranial magnetic resonance imaging showed pathological contrasts in the cortical regions involving the left hemisphere and in the leptomeningeal structures. We aim to present the case of an infant with SWS, which unlike the classical form was unidentifiable in physical examination and diagnosed using imaging methodsen_US
dc.identifier.doi10.4274/jpr.44265
dc.identifier.endpage105en_US
dc.identifier.issn2147-9445
dc.identifier.issn2587-2478
dc.identifier.issue2en_US
dc.identifier.startpage103en_US
dc.identifier.urihttps://doi.org/10.4274/jpr.44265
dc.identifier.urihttps://app.trdizin.gov.tr//makale/TXpBek9USTNOdz09
dc.identifier.urihttps://hdl.handle.net/11454/66501
dc.identifier.volume5en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofThe Journal of Pediatric Researchen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPediatrien_US
dc.titleSturge-Weber Syndrome Type IIIen_US
dc.typeArticleen_US

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