Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009 - PubMed
doi: 10.1111/j.1528-1167.2010.02522.x. Epub 2010 Feb 26.
Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern, Solomon L Moshé, Douglas Nordli, Perrine Plouin, Ingrid E Scheffer
Affiliations
- PMID: 20196795
- DOI: 10.1111/j.1528-1167.2010.02522.x
Free article
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009
Anne T Berg et al. Epilepsia. 2010 Apr.
Free article
Abstract
The International League Against Epilepsy (ILAE) Commission on Classification and Terminology has revised concepts, terminology, and approaches for classifying seizures and forms of epilepsy. Generalized and focal are redefined for seizures as occurring in and rapidly engaging bilaterally distributed networks (generalized) and within networks limited to one hemisphere and either discretely localized or more widely distributed (focal). Classification of generalized seizures is simplified. No natural classification for focal seizures exists; focal seizures should be described according to their manifestations (e.g., dyscognitive, focal motor). The concepts of generalized and focal do not apply to electroclinical syndromes. Genetic, structural-metabolic, and unknown represent modified concepts to replace idiopathic, symptomatic, and cryptogenic. Not all epilepsies are recognized as electroclinical syndromes. Organization of forms of epilepsy is first by specificity: electroclinical syndromes, nonsyndromic epilepsies with structural-metabolic causes, and epilepsies of unknown cause. Further organization within these divisions can be accomplished in a flexible manner depending on purpose. Natural classes (e.g., specific underlying cause, age at onset, associated seizure type), or pragmatic groupings (e.g., epileptic encephalopathies, self-limited electroclinical syndromes) may serve as the basis for organizing knowledge about recognized forms of epilepsy and facilitate identification of new forms.
Comment in
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Ferrie CD. Ferrie CD. Epilepsia. 2010 Apr;51(4):713-4. doi: 10.1111/j.1528-1167.2010.02540.x. Epilepsia. 2010. PMID: 20394642 No abstract available.
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What is a classification essay?
Fisher RS. Fisher RS. Epilepsia. 2010 Apr;51(4):714-5. doi: 10.1111/j.1528-1167.2010.02541.x. Epilepsia. 2010. PMID: 20394643 No abstract available.
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Shinnar S. Shinnar S. Epilepsia. 2010 Apr;51(4):715-7. doi: 10.1111/j.1528-1167.2010.02542.x. Epilepsia. 2010. PMID: 20394644 No abstract available.
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Wolf P. Wolf P. Epilepsia. 2010 Apr;51(4):717-8. doi: 10.1111/j.1528-1167.2010.02529.x. Epilepsia. 2010. PMID: 20394645 No abstract available.
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Guerrini R. Guerrini R. Epilepsia. 2010 Apr;51(4):718-20. doi: 10.1111/j.1528-1167.2010.02530.x. Epilepsia. 2010. PMID: 20394646 No abstract available.
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A sound conceptual framework for an epilepsy classification is still lacking.
Avanzini G. Avanzini G. Epilepsia. 2010 Apr;51(4):720-2. doi: 10.1111/j.1528-1167.2010.02531.x. Epilepsia. 2010. PMID: 20394647 No abstract available.
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Acute symptomatic seizures--should we retain the term?
Shorvon S, Guerrini R. Shorvon S, et al. Epilepsia. 2010 Apr;51(4):722-3. doi: 10.1111/j.1528-1167.2010.02501.x. Epilepsia. 2010. PMID: 20394648 No abstract available.
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Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies.
Mulley JC, Heron SE, Dibbens LM. Mulley JC, et al. Epilepsia. 2011 Mar;52(3):649-50. doi: 10.1111/j.1528-1167.2010.02953.x. Epilepsia. 2011. PMID: 21395569 No abstract available.
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