Learn how personalized genetic therapy helped researchers treat two children with a rare form of epilepsy, enabling one to ...

SCN2A-related developmental epileptic encephalopathy (DEE) is a rare, severe form of childhood epilepsy and one of the most ...

Around the world, over 50 million people are thought to be affected by epilepsy. However, despite the many affected, there is ...

SCN2A‑related developmental epileptic encephalopathy (DEE) is a rare, severe form of childhood epilepsy and one of the most ...

ORLANDO — Genetic testing is warranted in patients with epilepsy of unknown origin, new research suggests. Investigators found that pathogenic genetic variants were identified in over 40% of patients ...

Researchers have uncovered a novel biological pathway that can lead to seizures when disrupted. The findings also provide a ...

Researchers have uncovered a novel biological pathway that can lead to seizures when disrupted. The findings also provide a ...

Researchers have identified a potential treatment target for a genetic type of epilepsy. Researchers at the Francis Crick Institute, UCL and MSD have identified a potential treatment target for a ...

Epilepsy affects more than 50 million people worldwide, making it one of the most common neurological disorders. Although ...

Share on Pinterest More than 3 million people in the United States are living with epilepsy. © Marco Bottigelli/Getty Images Specific changes in DNA may increase the ...

Zakiya: When Massachusetts resident Ravit had her first son, Nadav, she remembers that he was deeply observant – even as an infant. Ravit: I used to look at him and think he's going to be a profound ...

As advances in genetic medicine create new opportunities for patients with rare diseases, congenital anomalies, developmental disabilities, epilepsy, inherited cancers, and other conditions, Start ...