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WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.

Karen L OliverMarina TrivisanoSimone A MandelstamAngela De DominicisDavid I FrancisTimothy E GreenAlison M MuirApoorva ChowdharyChristoph HertzbergKlaus GoldhahnJulia MetreauChristine PragerJason PinnerMichael CardamoneKenneth A MyersRichard J LeventerGaëtan LescaMelanie BahloMichael S HildebrandHeather C MeffordAngela M KaindlNicola SpecchioIngrid Eileen Scheffer
Published in: Epilepsia (2023)
Biallelic WWOX pathogenic variants cause an early infantile developmental and epileptic encephalopathy syndrome. The most common seizure types are focal seizures and epileptic spasms. Mortality risk is associated with mutation type; patients with biallelic null WWOX pathogenic variants have significantly lower survival probability compared to those carrying at least one presumed hypomorphic missense pathogenic variant.
Keyphrases
  • intellectual disability
  • copy number
  • early onset
  • autism spectrum disorder
  • case report
  • gene expression
  • dna methylation