Self-limited epilepsies in childhood

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Identification of epilepsy electroclinical syndromes is important to determine potential etiologies, preferred treatments, possible comorbidities, and expected outcomes. However, atypical features can make classification challenging but does not exclude classification. Childhood epilepsy with centrotemporal spikes is a self-limited and pharmaco-responsive epilepsy. However, there are many overlapping features with childhood-onset epileptic encephalopathies, such as Landau-Kleffner syndrome and epileptic encephalopathy with continuous spike-and-wave during sleep syndromes. Therefore, a careful history and additional evaluation are warranted for children who present with atypical features.

Original languageEnglish (US)
Title of host publicationEpilepsy Case Studies
Subtitle of host publicationPearls for Patient Care: Second Edition
PublisherSpringer International Publishing
Pages29-34
Number of pages6
ISBN (Electronic)9783030590789
ISBN (Print)9783030590772
DOIs
StatePublished - Dec 19 2020

Keywords

  • Benign rolandic epilepsy
  • Childhood epilepsy with centrotemporal spikes
  • Drug-resistant epilepsy
  • Focal epilepsy
  • Self-limited childhood epilepsy

ASJC Scopus subject areas

  • General Medicine

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