SE-ATLAS

Epilepsy with eyelid myoclonia Infantile spasms syndrome Epilepsy-telangiectasia syndrome Continuous spikes and waves during sleep Benign partial infantile seizures Neonatal epilepsy syndrome Rolandic epilepsy-speech dyspraxia syndrome Benign occipital epilepsy Childhood-onset epilepsy syndrome Progressive myoclonic epilepsy Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Dravet syndrome Lennox-Gastaut syndrome Epilepsy syndrome Landau-Kleffner syndrome Rare disorder with dystonia and other neurologic or systemic manifestation Sturge-Weber syndrome Infantile epilepsy syndrome Acute encephalopathy with inflammation-mediated status epilepticus Generalized epilepsy with febrile seizures-plus Non-specific early-onset epileptic encephalopathy Rare epilepsy Rare movement disorder Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Isolated dystonia Hemidystonia-hemiatrophy syndrome Combined dystonia Familial infantile myoclonic epilepsy Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression DEND syndrome Myoclonic epilepsy of infancy Idiopathic hemiconvulsion-hemiplegia syndrome Epilepsy with myoclonic absences Progressive myoclonic epilepsy with dystonia Myoclonic epilepsy in non-progressive encephalopathies Perioral myoclonia with absences Rare dystonia Myoclonic-astatic epilepsy Early-onset progressive encephalopathy with migrant continuous myoclonus Infantile spasms-broad thumbs syndrome Familial partial epilepsy Cryptogenic late-onset epileptic spasms Epilepsie réflexe Encéphalopathie liée à STXBP1 Trouble du déficit en CDKL5 Encéphalopathie épileptique et développementale associée à SYNGAP1