Rare yet debilitating disorders, Dravet syndrome, and other developing epileptic encephalopathies induce a variety of symptoms in children, such as seizures, intellectual incapacity, and even unexpected death. The majority of cases are brought on by a genetic mutation; variations in the sodium channel gene SCN1A are most frequently the cause […]
Epilepsy
Numerous treatments are being developed to target the genes causing the more than 100 epilepsies that have been linked to a single gene mutation.
Research establishes foundation for clinical experiment targeted at averting brain tumours in kids with NF1.
