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 language | English (US) |
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Title of host publication | Epilepsy Case Studies |
Subtitle of host publication | Pearls for Patient Care: Second Edition |
Publisher | Springer International Publishing |
Pages | 29-34 |
Number of pages | 6 |
ISBN (Electronic) | 9783030590789 |
ISBN (Print) | 9783030590772 |
DOIs | |
State | Published - 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