Progress in unraveling the genetic etiology of rolandic epilepsy

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Progress in unraveling the genetic etiology of rolandic epilepsy

Rolandic epilepsy (RE), or benign epilepsy of childhood with centrotemporal spikes (BECT), is the most frequent idiopathic partial epilepsy syndrome of childhood, where the "idiopathic" implies a genetic predisposition. Although RE has long been presumed to have a genetic component, clinical and genetic studies have shown a complex inheritance pattern. Furthermore, the underlying major genetic ...

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Todd Paralysis in Rolandic Epilepsy

Investigators from University of Gaziantep, Turkey described the clinical and EEG findings of patients with benign epilepsy of childhood with centrotemporal spikes (BECTS) experiencing postictal Todd paralysis.

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Benign rolandic epilepsy: neuropsychological findings

Benign rolandic epilepsy (BRE) is a partial idiopathic epilepsy of childhood presenting with a nocturnal seizure and with a typical EEG showing centrotemporal spike and multifocal or generalized sharp slow waves. Although normal neurological and intellectual development are expected in BRE, it is not infrequent to detect subtle defects in neuropsychological functions and neuromotor development....

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[Rolandic discharges in childhood epilepsy: magnetoencephalographic diagnosis].

INTRODUCTION Whole head magnetoencephalography (MEG) systems facilitate simultaneous recording from the entire brain surface and deep structures. Thus MEG may be accepted as a clinically feasible method for the evaluation of epileptic patients not diagnosed with EEG. CLINICAL CASE A 11 year old female, with tonic generalized seizures since birth. At the present time, seizures consist of initi...

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ژورنال

عنوان ژورنال: Seizure

سال: 2017

ISSN: 1059-1311

DOI: 10.1016/j.seizure.2017.02.012