Genetic heterogeneity in infantile spasms

EuroEPINOMICS-RES NLES working group, Sarah Weckhuysen

Research output: Contribution to journalArticlepeer-review

Abstract

Infantile spasms (IS) is a developmental and epileptic encephalopathy with heterogeneous etiologies including many genetic causes. Genetic studies have identified pathogenic variants in over 30 genes as causes of IS. Many of these genetic causes are extremely rare, with only one reported incidence in an individual with IS. To better understand the genetic landscape of IS, we used targeted sequencing to screen 42 candidate IS genes and 53 established developmental and epileptic encephalopathy genes in 92 individual with IS. We identified a genetic diagnosis for 7.6% of our cohort, including pathogenic variants in KCNB1 (n = 2), GNAO1 (n = 1), STXBP1 (n = 1), SLC35A2 (n = 1), TBL1XR1 (n = 1), and KIF1A (n = 1). Our data emphasize the genetic heterogeneity of IS and will inform the diagnosis and management of individuals with this devastating disorder.

Original languageEnglish
Pages (from-to)106181
JournalEpilepsy Research
Volume156
DOIs
Publication statusPublished - Oct 2019

Fingerprint Dive into the research topics of 'Genetic heterogeneity in infantile spasms'. Together they form a unique fingerprint.

Cite this