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Idiopathic Childhood Occipital Lobe Epilepsies in Turkish Children
Abstract
Purpose: Two forms of idiopathic occipital lobe epilepsy can be distinguished: an early onset or Panayiotopoulos type (PS), and a late onset or Gastaut type (GS). The aim of this study was to identify clinical manifestations and outcome in Turkish children with idiopathic occipital lobe epilepsy. Material and Methods: Thirty nine children (27 boys, 12 girls) were divided into the PS and GS type, according to the classification for epileptic seizures of the International League Against Epilepsy. Results: Among the 39 patients, 27 (69.3%) were boys and 12 (30.7%) were girls and the mean age at the seizure onset was 77.38 ± 27.33 months (36-145 months). The PS type patients consisted of 27 children (19 boys, 8 girls). The average age of seizure onset in PS type patients was 60.76 ± 14.21 months (range, 36-94 months). The GS type patients consisted of 12 children (8 boys, 4 girls), and seizure onset was 107.7 ± 18.8 months (range, 72-145 months). Ictal vomiting was more common in the PS type patients, and visual symptoms were more common in the GS type patients. We detected that after treatment, 27 patients (100%) in PS type and 10 patients (83.3%) in GS type became seizures-free. Two patients continued having seizures in GS type. Conclusions: The average age of seizure onset was much younger in the PS than in the GS. Also, in idiopathic occipital lobe epilepsy, the PS type has better seizure-free and prognosis than the GS.
Keywords
Kaynakça
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Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
-
Yayımlanma Tarihi
30 Eylül 2015
Gönderilme Tarihi
30 Eylül 2015
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 1970 Cilt: 40 Sayı: 3
MLA
İncecik, Faruk, vd. “Idiopathic Childhood Occipital Lobe Epilepsies in Turkish Children”. Cukurova Medical Journal, c. 40, sy 3, Ekim 2015, ss. 504-9, doi:10.17826/cutf.50852.
Cited By
İlkokul öğretmenlerinin epilepsi konusunda bilgi, tutum ve davranışları
Cukurova Medical Journal (Çukurova Üniversitesi Tıp Fakültesi Dergisi)
https://doi.org/10.17826/cukmedj.237491
