Efficacy of Dravet Syndrome Treatments in a Subset of Individuals with 2q24.3 Deletion: A-5 Patient Case Series
Published online on January 21, 2026
Abstract
Journal of Child Neurology, Ahead of Print.
Dravet syndrome (DS) is a developmental and epileptic encephalopathy often resulting from haploinsufficiency of the voltage-gated sodium channel (VGSC) geneSCN1Alocated on chromosome 2q24.3. Although single-nucleotide changes account for the majority of ...
Dravet syndrome (DS) is a developmental and epileptic encephalopathy often resulting from haploinsufficiency of the voltage-gated sodium channel (VGSC) geneSCN1Alocated on chromosome 2q24.3. Although single-nucleotide changes account for the majority of ...