| Literature DB >> 35503717 |
Nicola Specchio1, Elaine C Wirrell2, Ingrid E Scheffer3, Rima Nabbout4, Kate Riney5,6, Pauline Samia7, Marilisa Guerreiro8, Sam Gwer9, Sameer M Zuberi10, Jo M Wilmshurst11, Elissa Yozawitz12, Ronit Pressler13, Edouard Hirsch14, Sam Wiebe15, Helen J Cross16, Emilio Perucca17,18, Solomon L Moshé19, Paolo Tinuper20,21, Stéphane Auvin22.
Abstract
The 2017 International League Against Epilepsy classification has defined a three-tier system with epilepsy syndrome identification at the third level. Although a syndrome cannot be determined in all children with epilepsy, identification of a specific syndrome provides guidance on management and prognosis. In this paper, we describe the childhood onset epilepsy syndromes, most of which have both mandatory seizure type(s) and interictal electroencephalographic (EEG) features. Based on the 2017 Classification of Seizures and Epilepsies, some syndrome names have been updated using terms directly describing the seizure semiology. Epilepsy syndromes beginning in childhood have been divided into three categories: (1) self-limited focal epilepsies, comprising four syndromes: self-limited epilepsy with centrotemporal spikes, self-limited epilepsy with autonomic seizures, childhood occipital visual epilepsy, and photosensitive occipital lobe epilepsy; (2) generalized epilepsies, comprising three syndromes: childhood absence epilepsy, epilepsy with myoclonic absence, and epilepsy with eyelid myoclonia; and (3) developmental and/or epileptic encephalopathies, comprising five syndromes: epilepsy with myoclonic-atonic seizures, Lennox-Gastaut syndrome, developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep, hemiconvulsion-hemiplegia-epilepsy syndrome, and febrile infection-related epilepsy syndrome. We define each, highlighting the mandatory seizure(s), EEG features, phenotypic variations, and findings from key investigations.Entities:
Keywords: Landau-Kleffner syndrome; Lennox-Gastaut syndrome; Panayiotopoulos syndrome; benign occipital epilepsy; childhood epilepsy with centrotemporal spikes; continuous spike-and-wave in sleep; eyelid myoclonia; febrile infection-related epilepsy syndrome; hemiconvulsion-hemiplegia-epilepsy syndrome; myoclonic absences; myoclonic atonic
Mesh:
Year: 2022 PMID: 35503717 DOI: 10.1111/epi.17241
Source DB: PubMed Journal: Epilepsia ISSN: 0013-9580 Impact factor: 5.864