SE-ATLAS

Benign childhood occipital epilepsy, Gastaut type Chromosomal anomaly with epilepsy as a major feature Neurocutaneous syndrome with epilepsy Familial temporal lobe epilepsy Malignant migrating focal seizures of infancy Monogenic disease with epilepsy Familial focal epilepsy with variable foci W syndrome Cerebral malformation with epilepsy Acute encephalopathy with inflammation-mediated status epilepticus Early-onset epilepsy-intellectual disability-brain anomalies syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Metabolic diseases with epilepsy Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Familial mesial temporal lobe epilepsy with febrile seizures Cerebral diseases of vascular origin with epilepsy Celiac disease-epilepsy-cerebral calcification syndrome Epileptic encephalopathy with global cerebral demyelination Metal transport or utilization disorder with epilepsy Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Non-specific early-onset epileptic encephalopathy PEHO-like syndrome Female restricted epilepsy with intellectual disability PEHO syndrome Generalized epilepsy with febrile seizures-plus Rare epilepsy Moynahan syndrome Autosomal dominant epilepsy with auditory features Other metabolic disease with epilepsy Mesial temporal lobe epilepsy with hippocampal sclerosis ARX-related epileptic encephalopathy Oculocerebrocutaneous syndrome CNTNAP2-related developmental and epileptic encephalopathy Severe neonatal-onset encephalopathy with microcephaly Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Epilepsy and/or ataxia with myoclonus as a major feature Familial infantile myoclonic epilepsy Audiogenic seizures Progressive myoclonic epilepsy with dystonia Early infantile epileptic encephalopathy DEND syndrome Idiopathic hemiconvulsion-hemiplegia syndrome Early myoclonic encephalopathy Startle epilepsy Myoclonic epilepsy of infancy Thinking seizures Action myoclonus-renal failure syndrome Generalized epilepsy-paroxysmal dyskinesia syndrome Juvenile absence epilepsy Epilepsy with myoclonic absences Epilepsie myoclono-astatique Convulsions néonatales bénignes idiopathiques Encéphalopathie progressive précoce avec crises myocloniques migrantes et continues Epilepsie myoclonique des encéphalopathies non-progressives Epilepsie infantile familiale bénigne Epilepsie myoclonique juvénile Epilepsie rolandique Convulsions néonatales-infantiles bénignes familiales Syndrome de spasmes infantiles-pouces larges Encéphalopathie épileptique associée à KCNQ2 Epilepsie partielle familiale Epilepsie frontale à crises nocturnes autosomique dominante Epilepsie-absence de l'enfance Epilepsie partielle bénigne du nourrisson avec crises généralisées secondaires Syndrome d'épilepsie-microcéphalie-dysplasie squelettique Encéphalopathie épileptique-dyskinétique infantile Epilepsie néonatale bénigne familiale Syndrome des spasmes infantiles Epilepsie bénigne partielle de l'enfant avec crises partielles complexes Syndrome d'épilepsie-télangiectasie Syndrome des pointes-ondes continues du sommeil Trouble du déficit en CDKL5 Epilepsie partielle bénigne de l'adolescent Convulsions infantiles partielles bénignes Epilepsie temporale mésiale familiale bénigne Syndrome d'épilepsie liée à l'X-difficulté d'apprentissage-troubles du comportement Epilepsie à pointes occipitales Syndrome épileptique du nourrisson Syndrome épileptique du nouveau-né Syndrome épileptique de l'adolescence Syndrome de Dravet Epilepsie occipitale bénigne type Panayiotopoulos Syndrome épileptique Syndrome de convulsions infantiles-choréoathétose Dyskinésie paroxystique