Schizencephaly is a rare congenital anomaly with polymicrogyric gray matter-lined clefts [1–3]. Along with polymicrogyria, schizencephaly belongs to a group of malformations of cortical development occurring at the stage of neuronal organization [2, 4]. Patients with malformations of cortical development have a high prevalence of epilepsy, and many cases are medically refractory [5–7]. Although data from precise epidemiological studies are lacking, epilepsy has been reported in 37–74% of patients with schizencephaly [1, 8-10].
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