Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a rare and serious type of epilepsy. The first seizure often happens with a high fever and can last more …

Treatment challenges in patients with Dravet syndrome (DS). ASMs anti-seizure medications Another challenge is that some anti-seizure medications (ASMs) can exacerbate seizures in …

What is Dravet syndrome? Dravet syndrome is a rare, genetic epileptic encephalopathy that gives rise to seizures that don’t respond well to seizure medications. It begins in the first year of life …

What is Dravet syndrome? Dravet Syndrome is More than Seizures Dravet syndrome, previously known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a medication-resistant …

Someone who has Dravet Syndrome will experience a different pattern of seizures throughout their life, depending on their age. This section provides an overview of the seizures associated …

Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with …

Dravet syndrome is a rare and lifelong form of epilepsy that begins in the first year of life with frequent and/or prolonged seizures. The early seizures often happen when the infant has a …

Dravet Syndrome is a rare, genetic epileptic encephalopathy that can cause seizures that don’t respond well to seizure medications. It begins in the first year of life in an otherwise healthy …

Disease Overview Dravet syndrome (DS) is a severe form of epilepsy characterized by frequent, prolonged seizures often triggered by high body temperature (hyperthermia), developmental …

Dravet syndrome Dravet syndrome is a rare and complex epilepsy syndrome with frequent and difficult to treat seizures. Dravet syndrome typically starts in the first year of life in a normal …