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Phenytoin as a last-resort treatment in SCN8A encephalopathy.
Braakman, Hilde M; Verhoeven, Judith S; Erasmus, Corrie E; Haaxma, Charlotte A; Willemsen, Marjolein H; Schelhaas, H Jurgen.
Afiliación
  • Braakman HM; Department of Neurology Academic Center for Epileptology Kempenhaeghe and Maastricht UMC+Heeze the Netherlands.
  • Verhoeven JS; Department of Neurology Academic Center for Epileptology Kempenhaeghe and Maastricht UMC+Heeze the Netherlands.
  • Erasmus CE; Department of Neurology Radboud University Medical Center Nijmegen the Netherlands.
  • Haaxma CA; Department of Neurology Radboud University Medical Center Nijmegen the Netherlands.
  • Willemsen MH; Department of Human Genetics Radboud University Medical Center Donders Institute for Brain, Cognition and Behavior Nijmegen the Netherlands.
  • Schelhaas HJ; Department of Human Genetics Maastricht University Medical Center+Maastricht the Netherlands.
Epilepsia Open ; 2(3): 343-344, 2017 09.
Article en En | MEDLINE | ID: mdl-29588963
ABSTRACT
SCN8A encodes Nav1.6, one of the main voltage-gated sodium channel subunits in the brain, and SCN8A mutations lead to epileptic encephalopathy. Particular mutations render the mutant channel more susceptible to inhibition by phenytoin. Yet, the potentially severe side effects of phenytoin maintenance therapy, especially cognitive impairment, are undesirable in these already cognitively impaired patients. We describe a 5-year-old patient with SCN8A encephalopathy in whom phenytoin proved successful as emergency treatment to prevent clustering of seizures and status epilepticus, thus hospital stays. The ketogenic diet, levetiracetam, zonisamide, topiramate, and phenytoin maintenance therapy resulted in adverse reactions not previously documented in SCN8A encephalopathy.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Epilepsia Open Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Epilepsia Open Año: 2017 Tipo del documento: Article