Lacosamide for SCN2A-related intractable neonatal and infantile seizures

Flor Hirsch Hadar, Heyman Eli, Livneh Ayelet, Reish Orit, Watemberg Nathan, Litmanovits Ita, Ben Sason Lilli Anat, Lev Dorit, Lerman Sagie Tally, Bassan Haim*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

31 Scopus citations


Voltage-gated sodium channel alpha subunit 2 (SCN2A) gene mutations are associated with neonatal seizures and a wide range of epilepsy syndromes. Previous reports suggest that traditional sodium channel blockers (SCBs) such as phenytoin, carbamazepine, and lamotrigine have a beneficial effect on SCN2A-related neonatal seizures, as they counteract the gain-of-function effect of mutated Nav1.2 channels. Additionally, SCBs are beneficial against other sodium and potassium channel-related neonatal seizures. There are, however, few reports describing the effect of the new SCB lacosamide against neonatal and infantile epileptic seizures. We report herein two neonates with intractable neonatal seizures with SCN2A pathogenic missense variants. Both infants showed temporary seizure relief following IV administrations of phenytoin, but were resistant to a combination of antiepileptic drugs, while complete seizure control was achieved following lacosamide administration. We suggest that SCBs, e.g. phenytoin, should be introduced early for refractory neonatal seizures of non-lesional and presumably genetic origin. If any beneficial response to a SCB is noted, this should prompt an initiation of additional SCBs. New clinical trials will provide data on the efficacy and safety of the new SCB lacosamide for genetic neonatal seizures and perhaps neonatal seizures in general.

Original languageEnglish
Pages (from-to)440-446
Number of pages7
JournalEpileptic Disorders
Issue number5
StatePublished - Oct 2018


  • SCN2A
  • infantile
  • intractable
  • lacosamide
  • neonatal
  • seizure
  • sodium channel blocker


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