Since New Year's Eve 2019, this "happy" and "positive" little girl has suffered a seizure almost every day. Poppy Whinney was ...

Dravet Syndrome occurs in around one in every 15,000 live births and is among the most treatment-resistant genetic epilepsies.

Lucy Murphy says she wanted to raise awareness of Dravet Syndrome - a rare form of epilepsy.

‘Life-changing’ results for children with severe epilepsy in pioneering drug trial Children with Dravet syndrome have taken part in a clinical trial at Sheffield Children’s Hospital ...

Dravet syndrome (DS) is a rare and severe form of epilepsy that causes intellectual disability and motor deficits and can lead to premature death. A loss-of-function mutation in one copy of SCN1A, ...

M and D's son, B, was born with a seizure disorder they would later learn was Dravet syndrome.

Jim Brennan and McKelvey Homes have raised more than $2.5 million in six years to support research for Dravet Syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI).

Dravet syndrome is a severe form of epilepsy, usually diagnosed in infancy, that is associated with developmental delays and severe seizures.

SEATTLE, Wash. -- Scientists at the Allen Institute have made a major breakthrough in research for people living with Dravet Syndrome, which is a rare and debilitating form of epilepsy ...

Scientists developed a promising gene replacement therapy for Dravet syndrome in mice. The therapy alleviated symptoms without toxicity or side effects, marking a significant step forward in treating ...

By replacing the defective gene associated with Dravet syndrome in mice, scientists successfully alleviated symptoms without side effects.