Article
Modifying genetic epilepsies – Results from studies on tuberous sclerosis complex
6 Dec 2019
Abstract excerpt
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder affecting approximately 1 in 6,000 in general population and represents one of the most common genetic causes of epilepsy. Epilepsy affects 90% of the patients and appears in the first 2 years of life in the majority of them. Early onset of epilepsy in the first year of life is associated with high risk of cognitive decline and...
Topics
Join the communities discussing this publication.