AdHave A Patient With Symptoms Of DravetSyndrome? Learn About The Steps To Prescribing. Contact A Representative To Learn More About A Treatment For DravetSyndrome.
My infant has received genetic test results indicating an SCN1A mutation. What does this mean?
A:
In years past, a mutation in the SCN1A gene has confirmed a diagnosis of Dravet syndrome in patients that were already showing the typical disease progression. When access to...
AdDravetSyndrome Is A Rare Form Of Epilepsy. Learn More About Treating DravetSyndrome. Explore Safety, Efficacy, And Treatment Results. View Treatment Data For Patients.