SE-ATLAS

Acute encephalopathy with inflammation-mediated status epilepticus Benign occipital epilepsy Benign partial infantile seizures Childhood-onset epilepsy syndrome Combined dystonia Continuous spikes and waves during sleep Cryptogenic late-onset epileptic spasms DEND syndrome Dravet syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Early-onset progressive encephalopathy with migrant continuous myoclonus Epilepsy syndrome Epilepsy with eyelid myoclonia Epilepsy with myoclonic absences Epilepsy-telangiectasia syndrome Familial infantile myoclonic epilepsy Familial partial epilepsy Generalized epilepsy with febrile seizures-plus Hemidystonia-hemiatrophy syndrome Idiopathic hemiconvulsion-hemiplegia syndrome Infantile epilepsy syndrome Infantile spasms syndrome Infantile spasms-broad thumbs syndrome Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Isolated dystonia Landau-Kleffner syndrome Lennox-Gastaut syndrome Myoclonic epilepsy in non-progressive encephalopathies Myoclonic epilepsy of infancy Myoclonic-astatic epilepsy Neonatal epilepsy syndrome Non-specific early-onset epileptic encephalopathy Perioral myoclonia with absences Progressive myoclonic epilepsy Progressive myoclonic epilepsy with dystonia Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Rare epilepsy Rare movement disorder Reflex epilepsy Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Rolandic epilepsy-speech dyspraxia syndrome STXBP1-related encephalopathy SYNGAP1-related developmental and epileptic encephalopathy Sturge-Weber syndrome