Title of article: Dravet syndrome Authors: Hossam Salameh, Yasmeen Dahabreh Organizers: Ainaa A.Alzamari, Hamid Ghanem Reviewer: Ethar Hazaimeh   Keywords: Dravet syndrome(DS), severe myoclonic epilepsy of infancy (SMEI), SCN1A, NAV1.1, Febrile seizures, sudden unexpected death in epilepsy (SUDEP), genetic epilepsy with febrile seizures plus (GEFS+), status epilepticus (SE), multiple anti-seizure medications (ASMs).                   Abstract Background: Dravet syndrome (DS) is a genetic refractory epilepsy, formerly known as severe myoclonic epilepsy of infancy. It is characterized by temperature-sensitive seizures, resistance to therapy, and developmental differences in children. Despite meeting developmental milestones before seizures, they show signs of autism spectrum features and developmental […]