WHAT IS DRAVET SYNDROME ?

Dravet syndrome is a rare form of epilepsy associated with neurological development disorders. The onset is during the first year of life in a normal developing child.

THE HISTORY OF DRAVET SYNDROME

Dravet Syndrome was first described in 1978 as « Severe Myoclonic Epilepsy in Infancy » (SMEI) by Dr Charlotte DRAVET but has been recognized throughout the world since then.

Real life: Clinical cases - Preview