Idiopathic childhood occipital epilepsy of Gastaut information
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Idiopathic childhood occipital epilepsy of Gastaut (ICOE-G) is a pure but rare form of idiopathic occipital epilepsy that affects otherwise normal children and adolescents.[1] It is classified amongst benign idiopathic childhood focal epilepsies such as rolandic epilepsy and Panayiotopoulos syndrome.[2]
^Caraballo, Roberto; Koutroumanidis, Michael; Panayiotopoulos, Chrysostomos P.; Fejerman, Natalio (2 December 2009). "Idiopathic Childhood Occipital Epilepsy of Gastaut: A Review and Differentiation From Migraine and Other Epilepsies". Journal of Child Neurology. 24 (12): 1536–1542. doi:10.1177/0883073809332395. PMID 19955346. S2CID 206547729.
^Panayiotopoulos, C. P.; Michael, M.; Sanders, S.; Valeta, T.; Koutroumanidis, M. (21 August 2008). "Benign childhood focal epilepsies: assessment of established and newly recognized syndromes". Brain. 131 (9): 2264–2286. doi:10.1093/brain/awn162. PMID 18718967.
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