Neonatal and Infantile Onset: CDKL5-DEE, Dravet syndrome, Genetic epilepsy with febrile seizures +, Sturge-Weber syndrome, Pyridoxine-dependent developmental and epileptic encephalopathy, Gelastic seizures with hypothalamic hamartoma, Glucose transporter 1 deficiency syndrome, Childhood Onset: DEE-SWAS, epilepsy with eyelid myoclonia, epilepsy with myoclonic absences, epilepsy with myoclonic-atonic seizures, Lennox-Gastaut syndrome, Hemiconvulsion-hemiplegia syndrome, Self-limited epilepsy with autonomic seizures, Variable Age Onset: Epilepsy with auditory features, sleep-related hypermotor epilepsy, epilepsy with reading-induced seizures, familial focal epilepsy with variable foci, familial mesial temporal lobe epilepsy, progressive myoclonus epilepsies, Rasmussen syndrome,

Epilepsy Syndromes: Sort the Syndromes into the Correct Age Group

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