Syndromic classification of patients with typical absence seizures

Arq Neuropsiquiatr. 2003 Sep;61(3A):580-7. doi: 10.1590/s0004-282x2003000400010. Epub 2003 Sep 16.

Abstract

The aim of this study is to compare ILAE classification (1989) and Panayiotopoulos' criteria (1997) for absence epilepsies. We studied 455 typical absences (ILAE, 1981) by video-EEG in 43 patients with normal neurological and neuroradiological examinations and interictal EEG with spike-wave complexes higher than 2.5Hz. Syndromic diagnosis was possible in 60.5% and 67.4% of the patients using ILAE classification and Panayiotopoulos' proposal, respectively. According to ILAE criteria 19 patients had childhood absence epilepsy (CAE), five juvenile absence epilepsy (JAE), one juvenile myoclonic epilepsy (JME) and one epilepsy with specific modes of seizure precipitation. According to Panayiotopoulos' proposal, 10 had CAE, 14 JAE, one JME, three myoclonic absence epilepsy and one eyelid myoclonia with absences. We conclude that Panayiotopoulos' criteria and ILAE classification for absence epilepsies, which did not allow for the classification of 32.6% and 39.5% of cases, respectively, were still insufficient to classify all patients under specific diagnosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Child
  • Child, Preschool
  • Electroencephalography
  • Epilepsies, Myoclonic / classification*
  • Epilepsies, Myoclonic / physiopathology
  • Epilepsy, Absence / classification*
  • Epilepsy, Absence / physiopathology
  • Follow-Up Studies
  • Humans
  • Infant
  • Middle Aged
  • Myoclonic Epilepsy, Juvenile / diagnosis
  • Syndrome
  • Video Recording