Dravet Syndrome is a rare and severe form of epilepsy that typically begins in the first year of life. It is characterized by prolonged seizures, often triggered by fever or overheating. Children with Dravet Syndrome may experience developmental delays and have a higher risk of other health issues. The condition is usually caused by mutations in the SCN1A gene, which affects sodium channels in the brain. Treatment often involves a combination of medications and therapies, but managing seizures can be challenging. Early diagnosis and intervention are crucial for improving outcomes for affected individuals.