Aim: To determine the long-term probability of remission without antiepileptic treatment of common epileptic syndromes and of children without a specific syndromic diagnosis.
Patients And Methods: All children less than 14 years old with 2 or more unprovoked seizures seen at our hospital between June 1, 1994, and March 1, 2011 (n = 680), were included and prospectively followed up until August 15, 2020. Syndromic diagnosis was made retrospectively but blinded to subsequent evolution, employing the data available at 6 months after diagnosis and under predefined operational criteria.
Introduction: Studies about childhood epilepsy with centrotemporal spikes (CECTS), most of them retrospective, include patients with highly heterogeneous features.
Aim: To investigate the prognostic value of objective diagnostic criteria for CECTS applied at six month of evolution of epilepsy.
Patients And Methods: All patients with one or more unprovoked epileptic seizures (n = 827) were prospectively included.
It is estimated that about 70 million people all over the world suffer from epilepsy, half of which are children, in whom the prevalence is around 0.5 to 0.8%.
View Article and Find Full Text PDFIntroduction: Panayiotopoulos syndrome (PS) is an epileptic syndrome of childhood. Until now only a small number of studies have been published about this syndrome.
Aim: To study the frequency, semiology and prognosis of PS.
Introduction: Benign infantile epilepsy is an epileptic syndrome of infancy. Until now, only a small number of case-series have been published.
Aim: To study the frequency, semiology and prognosis of benign infantile epilepsy.