Assessment of cognitive and behavioral aspects in children with Rolandic Epilepsy (RE or Benign Epilepsy with Centro-Temporal Spikes / BECTS)
RE is the most common form of childhood epilepsy. It is caused by the hyperexcitability of a system of neurons in only one hemisphere without apparent brain injury or cerebral structural abnormalities (Capovilla et al., 2009), it is usually well controlled by medication and seizures disappear by adolescence. Although RE is still officially considered as a benign syndrome without cognitive impairments (Berg et Scheffer, 2011), a growing body of literature highlights the existence of a wide range of cognitive deficits (Sarco et al., 2011; Baglietto et al., 2001; Metz-Lutz et Filippini, 2006; Weglage, Demsky, Pietsch, et Kurlemann, 1997). In RE, we know that abnormal epileptic activity is found in central and temporal regions of the brain.