Congenital bilateral perisylvian syndrome

dc.contributor.authorYildirim, Hanefi
dc.contributor.authorKoc, Mustafa
dc.contributor.authorPoyraz, Kuersad
dc.contributor.authorOgur, Erkin
dc.contributor.authorKabakus, Nimet
dc.date.accessioned2026-08-12T17:00:54Z
dc.date.issued2008
dc.departmentFırat Üniversitesi
dc.description.abstractCongenital bilateral perisylvian syndrome is a structural malformation of the brain which normal pattern of folds on the surface of the brain is replaced with many small abnormal folds. The underlying anomaly is polymicrogyria, a malformation of the cerebral cortex. Polymicrogyria refers to excessive number of prominent and small convolutions composed from shallow and enlarged sulci. This anomaly constitutes lobular appearance of cerebral cortex. We present cranial magnetic resonance imaging (MRI) findings of a 3-year old male patient who was admitted with asymmetric facial paralysis, chewing and swallowing difficulties and intractable seizures. Brain MRI revealed bilateral perisylvian cortical dysplasia including polymicrogyria and local cortical thickening that extends to the level of vertex.
dc.identifier.endpage421
dc.identifier.issn1300-0292
dc.identifier.issn2146-9040
dc.identifier.issue3
dc.identifier.startpage419
dc.identifier.urihttps://hdl.handle.net/11508/47426
dc.identifier.volume28
dc.identifier.wosWOS:000257362400026
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherOrtadogu Ad Pres & Publ Co
dc.relation.ispartofTurkiye Klinikleri Tip Bilimleri Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectcongenital
dc.subjectbrain
dc.subjectepilepsy
dc.subjectrolandic
dc.subjectmagnetic resonance imaging
dc.titleCongenital bilateral perisylvian syndrome
dc.typeArticle

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