SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis

Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic encephalopathy. More than 1,800 mutations have been identified in SCN1A . Although it is known that SCN1A is the main cause of DS and... View More