Myoclonic Absence Seizures in Dravet Syndrome.

Abstract

BACKGROUND Dravet syndrome is a developmental and epileptic encephalopathy that occurs as a result of SCN1A mutations in more than 80% of affected individuals. The core clinical features of Dravet syndrome include febrile and afebrile seizures beginning before 12 months; multiple seizure types, usually medically refractory, including hemiclonic, generalized… (More)
DOI: 10.1016/j.pediatrneurol.2017.01.004

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Cite this paper

@article{Myers2017MyoclonicAS, title={Myoclonic Absence Seizures in Dravet Syndrome.}, author={Kenneth A Myers and Ingrid E. Scheffer}, journal={Pediatric neurology}, year={2017}, volume={70}, pages={67-69} }