Precision in pediatric epilepsy

F1000Res. 2019 Feb 6:8:F1000 Faculty Rev-163. doi: 10.12688/f1000research.16494.1. eCollection 2019.

Abstract

Epilepsy in infants and children is one of the most common and devastating neurological disorders. In the past, we had a limited understanding of the causes of epilepsy in pediatric patients, so we treated pediatric epilepsy according to seizure type. Now with new tools and tests, we are entering the age of precision medicine in pediatric epilepsy. In this review, we use the new etiological classification system proposed by the International League Against Epilepsy to review the advances in the diagnosis of pediatric epilepsy, describe new tools to identify seizure foci for epilepsy surgery, and define treatable epilepsy syndromes.

Keywords: autoimmune encephalitis; epilepsy gene panels; metabolic testing; whole exome sequencing; whole genome sequencing.

Publication types

  • Review

MeSH terms

  • Child
  • Epilepsy* / genetics
  • Epilepsy* / therapy
  • Humans
  • Infant
  • Precision Medicine*
  • Seizures

Grants and funding

The author(s) declared that no grants were involved in supporting this work.