Genetic epileptic encephalopathies: Is all written into the DNA?
Article first published online: 13 NOV 2013
Wiley Periodicals, Inc. © 2013 International League Against Epilepsy
Special Issue: Epileptic Encephalopathies: Proceedings of the International Sicilian Workshop, Sciacca, April 29–30, 2012
Volume 54, Issue Supplement s8, pages 22–26, November 2013
How to Cite
Striano, P., de Jonghe, P. and Zara, F. (2013), Genetic epileptic encephalopathies: Is all written into the DNA?. Epilepsia, 54: 22–26. doi: 10.1111/epi.12419
- Issue published online: 13 NOV 2013
- Article first published online: 13 NOV 2013
- Dravet syndrome;
Epileptic encephalopathy is a condition in which epileptic activity, clinical or subclinical, is thought to be responsible for any disturbance of cognition, behavior, or motor control. However, experimental evidence supporting this clinical observation are still poor and the causal relationship between pharmacoresistant seizures and cognitive outcome is controversial. In the past two decades, genetic studies shed new light onto complex mechanisms underlying different severe epileptic conditions associated with intellectual disability and behavioral abnormalities, thereby providing important clues on the relationship between seizures and cognitive outcome. Dravet syndrome is a childhood disorder associated with loss-of-function mutations in SCN1A and is characterized by frequent seizures and severe cognitive impairment, thus well illustrating the concept of epileptic encephalopathy. However, it is difficult to determine the causative role of the underlying sodium channel dysfunction and that of the consequent seizures in influencing cognitive outcome in these children. It is also difficult to demonstrate whether a recognizable profile of cognitive impairment or a definite behavioral phenotype exists. Data from the laboratory and the clinics may provide greater insight into the degree to which epileptic activity may contribute to cognitive impairment in individual syndromes.