Affiliation:
1. Department of Neurology and Developmental Pediatrics,
The Wolfson Centre, University of London, London, U.K.
Abstract
Epilepsy syndromes, defmed as clusters of symptoms or signs occurring consistently together, form the basis of the currently accepted classification of the epilepsies. The concept of epilepsy syndrome is practical for the diagnosis, prognosis, orientation of treatment, and selection of appropriate investigations, but it is of variable specificity and usually does not give information on causes and mechanisms of an epilepsy. Some syndromes, such as childhood absences, partial epilepsy with centrotemporal spikes, or juvenile myoclonic epilepsy, are precisely characterized while other syndromes such as grand mal on awakening or the multiple syndromes with myoclonic seizures are poorly delineated. The usefulness of the concept is limited to well-defined and generally accepted syndromes and many cases of epilepsy do not fit easily in recognizable syndromes. (J Child Neurol 1994; 9(Suppl):2S14-2S18).
Subject
Clinical Neurology,Pediatrics, Perinatology, and Child Health
Reference32 articles.
1. Masland RL: The classification of the epilepsies, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology, Vol 15, The Epilepsies. Amsterdam, North-Holland, 1974, pp 1-29.
2. Marsden CD, Reynolds EH: Neurology, in Laidlaw J, Richens A (eds): A Textbook of Epilepsy, 2nd ed. Edinburgh, Churchill Livingstone, 1983, pp 97-131.
3. Proposal for Revised Classification of Epilepsies and Epileptic Syndromes.
4. Aicardi J.: Epilepsy in Children, 2nd ed. New York, Raven Press, 1994, pp 9-17.
5. Hypothalamic hamartomas and ictal laughter: Evolution of a characteristic epileptic syndrome and diagnostic value of magnetic resonance imaging
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