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Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndrome.

Ingo HelbigGiulia BarciaManuela PendziwiatShiva GanesanStefanie H MuellerKatherine L HelbigPriya VaidiswaranJulie XianPeter D GalerZaid AfawiNicola SpecchioGerhard KlugerGregor KuhlenbäumerSilke AppenzellerMichael WittigUri KramerAndreas van BaalenRima Nabboutnull null
Published in: Annals of clinical and translational neurology (2020)
Febrile infection-related epilepsy syndrome (FIRES) is a devastating epilepsy characterized by new-onset refractory status epilepticus with a prior febrile infection. We performed exome sequencing in 50 individuals with FIRES, including 27 patient-parent trios and 23 single probands, none of whom had pathogenic variants in established genes for epilepsies or neurodevelopmental disorders. We also performed HLA sequencing in 29 individuals with FIRES and 529 controls, which failed to identify prominent HLA alleles. The genetic architecture of FIRES is substantially different from other developmental and epileptic encephalopathies, and the underlying etiology remains elusive, requiring novel approaches to identify the underlying causative factors.
Keyphrases
  • copy number
  • single cell
  • case report
  • urinary tract infection
  • genome wide
  • chemotherapy induced
  • bioinformatics analysis