Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions. Issue 6 (3rd May 2022)

• Record Type: Journal Article
• Authors: Wirrell, Elaine C.; Nabbout, Rima; Scheffer, Ingrid E.; Alsaadi, Taoufik; Bogacz, Alicia; French, Jacqueline A.; Hirsch, Edouard; Jain, Satish; Kaneko, Sunao; Riney, Kate; Samia, Pauline; Snead, O. Carter; Somerville, Ernest; Specchio, Nicola; Trinka, Eugen; Zuberi, Sameer M.; Balestrini, Simona; Wiebe, Samuel; Cross, J. Helen; Perucca, Emilio; Moshé, Solomon L.; Tinuper, Paolo
• Is Part Of: Epilepsia. Volume 63:Issue 6(2022)
• Page Start: 1333
• Page End: 1348
• Publication Date: 2022-05-03
• Subjects: developmental and epileptic encephalopathy -- electroencephalogram -- focal epilepsy -- idiopathic generalized epilepsy -- semiology; Epilepsy -- Periodicals; 616.853
• DOI: 10.1111/epi.17237
• Languages: English
• ISSNs: 0013-9580

Abstract

Abstract: Epilepsy syndromes have been recognized for >50 years, as distinct electroclinical phenotypes with therapeutic and prognostic implications. Nonetheless, no formally accepted International League Against Epilepsy (ILAE) classification of epilepsy syndromes has existed. The ILAE Task Force on Nosology and Definitions was established to reach consensus regarding which entities fulfilled criteria for an epilepsy syndrome and to provide definitions for each syndrome. We defined an epilepsy syndrome as "a characteristic cluster of clinical and electroencephalographic features, often supported by specific etiological findings (structural, genetic, metabolic, immune, and infectious)." The diagnosis of a syndrome in an individual with epilepsy frequently carries prognostic and treatment implications. Syndromes often have age‐dependent presentations and a range of specific comorbidities. This paper describes the guiding principles and process for syndrome identification in both children and adults, and the template of clinical data included for each syndrome. We divided syndromes into typical age at onset, and further characterized them based on seizure and epilepsy types and association with developmental and/or epileptic encephalopathy or progressive neurological deterioration. Definitions for each specific syndrome are contained within the corresponding position papers.