SE-ATLAS

W syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Metabolic diseases with epilepsy Cerebral malformation with epilepsy Inflammatory and autoimmune disease with epilepsy Acute encephalopathy with inflammation-mediated status epilepticus Cerebral diseases of vascular origin with epilepsy Infectious disease with epilepsy Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome PEHO-like syndrome Generalized epilepsy with febrile seizures-plus PEHO syndrome Rare epilepsy Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Moynahan syndrome Oculocerebrocutaneous syndrome Familial infantile myoclonic epilepsy CNTNAP2-related developmental and epileptic encephalopathy Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Action myoclonus-renal failure syndrome Myoclonic epilepsy of infancy Idiopathic hemiconvulsion-hemiplegia syndrome DEND syndrome Epilepsy with myoclonic absences Progressive myoclonic epilepsy with dystonia Myoclonic epilepsy in non-progressive encephalopathies Myoclonic-astatic epilepsy Early-onset progressive encephalopathy with migrant continuous myoclonus Febrile infection-related epilepsy syndrome Perioral myoclonia with absences Familial partial epilepsy Infantile spasms-broad thumbs syndrome Reflex epilepsy Epilepsy with eyelid myoclonia Cryptogenic late-onset epileptic spasms Infantile spasms syndrome Syndrome des pointes-ondes continues du sommeil Convulsions infantiles partielles bénignes Epilepsie à pointes occipitales Syndrome d'épilepsie rolandique-dyspraxie de la parole Syndrome épileptique du nouveau-né Syndrome d'épilepsie rolandique-dystonie paroxystique induite par l'effort-crampe de l'écrivain Syndrome épileptique de l'enfance Syndrome épileptique du nourrisson Epilepsie myoclonique progressive Syndrome épileptique de l'adolescence Syndrome de Dravet Syndrome épileptique Syndrome de Lennox-Gastaut Syndrome de Landau-Kleffner Syndrome neurocutané associé à une épilepsie Maladie monogénique avec épilepsie Anomalie chromosomique avec épilepsie comme manifestation majeure