The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.

Dravet Syndrome

Prevalence: 1/20000

neurological

Official·OMIM:607208 Official·ORPHA33069

Severe myoclonic epilepsy due to SCN1A gene mutations.

Associated Genes

SCN1ASodium Voltage-Gated Channel Alpha Subunit 1

Chromosome 2Autosomal Dominant