Congenital bilateral perisylvian syndrome: Differential diagnosis

dc.contributor.authorYildirim, Hanefi
dc.contributor.authorKoç, Mustafa
dc.contributor.authorPoyraz, Kürşad
dc.contributor.authorO?ur, Erkin
dc.contributor.authorKabakuş, Nimet
dc.date.accessioned2026-08-12T16:12:48Z
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. Copyright © 2008 by Türkiye Klinikleri.
dc.identifier.endpage421
dc.identifier.issn1300-0292
dc.identifier.issue3
dc.identifier.scopus2-s2.0-46749098294
dc.identifier.scopusqualityQ4
dc.identifier.startpage419
dc.identifier.urihttps://hdl.handle.net/11508/42668
dc.identifier.volume28
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherTurkiye Klinikleri
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectBrain; Congenital; Epilepsy, rolandic; Magnetic resonance imaging
dc.titleCongenital bilateral perisylvian syndrome: Differential diagnosis
dc.typeArticle

Dosyalar