EEG in Gastaut Type-Idiopathic Childhood Occipital Epilepsy.
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Published:
Sep 20, 2016
Keywords:
Gastaut type-idiopathic childhood occipital epilepsy; G-ICOE; EEG;Epilepsy; Idiopathic focal epilepsy
Main Article Content
Abstract
Gastaut type-idiopathic childhood occipital epilepsy (G-ICOE) is a rare form of idiopathic childhood occipital epilepsy. It is characterized by late-onset, brief, frequent, usually diurnal, elementary visual auras which may be associated with hemi-clonic or generalized convulsion. Occasionally the clinical presentation can be overlapped with Panayiotopoulos syndrome. Typical EEG findings are occipital paroxysms. The prognosis remains uncertain, but most seizures are often responsive to antiepileptic treatment.
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How to Cite
1.
Chansakul C. EEG in Gastaut Type-Idiopathic Childhood Occipital Epilepsy. BKK Med J [Internet]. 2016 Sep. 20 [cited 2024 Nov. 17];12(1):93. Available from: https://he02.tci-thaijo.org/index.php/bkkmedj/article/view/221579
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Case Report
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References
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2. Gastaut H. A new type of epilepsy: benign partial epilepsy of childhood with occipital spike-waves. Clin Electroen- cephalogr 1982;13:13-22.
3. Kivity S, Ephraim T, Weitz R, et al. Childhood epilepsy with occipital paroxysms: clinical variants in 134 patients. Epilepsia 2000;41:1522-33.
4. Taylor I, Berkovic SF, Kivity S, et al. Benign occipital epilepsies of childhood: clinical features and genetics. Brain 2008;131:2287-94.
5. Panayiotopoulos CP. Elementary visual hallucinations, blindness, and headache in idiopathic occipital epilepsy: differentiation from migraine. J Neurol Neurosurg Psy- chiatry 1999;66:536-40.
6. Caraballo RH, Cersósimo RO, Fejerman N. Childhood occipital epilepsy of Gastaut: a study of 33 patients. Epi- lepsia 2008;49:288-97.