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

The research, taking place at the Allen Institute for Brain Science, offers new hope to families fighting against Dravet Syndrome, a severe form of epilepsy that devastates childhood development.

“People who take drugs for epilepsy often complain that the drugs ... “Our goal is to be very precise, where we can deliver just the gene that's missing and really target the circuit.

In a groundbreaking advancement for families grappling with the challenges of Dravet syndrome, a rare and life-altering form ...

CDKL5, one of the five members of the CDKL family of genes, is important for proper neurodevelopment and associated with ...

Professor Lynch said genetic testing had shown that Sandra had a mutation ... The consultant said Sandra was likely to have ...

In a groundbreaking advancement for families grappling with the challenges of Dravet syndrome, a rare and life-altering form ...

New Approach to Epilepsy Treatment Combines Genetics and Brain Mapping Nov. 26, 2024 — Researchers have developed a new method called MoPEDE, which has the potential to improve epilepsy treatment.

A simple genomics blood test could improve treatment and care for childhood epilepsy, but more investment is needed to make ...

March is Cerebral Palsy Awareness Month. Dr. Paul Kruszka is Chief Medical Officer at GeneDx, a commercial laboratory ...

The FDA has granted Breakthrough Therapy designation to radiprodil for the treatment of seizures associated with GRIN-related neurodevelopmental disorder with GoF mutations.