Frequently identified genetic developmental and epileptic encephalopathy: A review focusing on precision medicine

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4 Citations (Scopus)

Abstract

In this article, we reviewed current knowledge regarding gene-specific therapies for some developmental and epileptic encephalopathy caused by genes with high diagnostic yields, and which are therefore, also more frequently encountered by physicians during treatment, including ALDH7A1, CDKL5, KCNQ2, KCNT1, SCN2A, SCN8A, STXBP1, and SYNGAP1. Among these therapies, the ones directly targeting causative mutations are retigabine in KCNQ2 encephalopathy and quinidine in KCNT1 encephalopathy. However, despite promising results in vitro, the outcomes related to these therapies were disappointing when administered to patients. Considering the pathologic mecha-nisms of causative mutations, sodium channel blockers are recommended for patients with KCNQ2 mutations, infantile epileptic encephalopathy patients with SCN2A mutations, and patients with SCN8A mutations. Levetiracetam can be considered for patients with STXBP1 mutations.

Original languageEnglish
Pages (from-to)2-12
Number of pages11
JournalAnnals of Child Neurology
Volume27
Issue number1
DOIs
Publication statusPublished - 2019 Mar

Bibliographical note

Publisher Copyright:
© 2019 Korean Child Neurology Society.

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology
  • Neurology

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