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Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood. Most children will outgrow the syndrome (it starts around the age of 3-13 with a peak around 8–9 years and stops around age 14-18), hence the label benign. With this condition, seizures affect the face and sometimes the body. It almost always disappears, though, by adolescence.
Journals Related to Rolandic Epilepsy
Brain Disorders & Therapy, Journal of Neurology & Neurophysiology, Journal of Neurological Disorders, Epilepsy Journal, Brain- A Journal of Neurology, British Journal of Research, Neurologic Clinics, Neuromuscular Disorders, Neuroscience, Journal of Child Neurology, Benign rolandic epilepsy: neuropsychological findings, Dipole tracing in childhood epilepsy with special reference to Rolandic epilepsy