Dravet syndrome is a severe genetic epilepsy that appears early in life. About 75 percent of cases can be attributed to mutations in the SCN1A gene encoding the sodium channel NaV1.1. The remaining patients with this syndrome are without a definitive molecular genetic diagnosis. Research...
Childhood vaccination is linked with earlier onset of the neurological disorder Dravet syndrome, finds a retrospective study. But vaccination should not be withheld from children with Dravet syndrome because vaccination before or after disease onset does not affect their clinical outlook...