SE-ATLAS

Benigne okzipitale Epilepsie des Kindesalters Typ Gastaut Chromosomenanomalie mit Epilepsie als Hauptmerkmal Neurokutanes Syndrom mit Epilepsie Temporallappenepilepsie, familiäre Maligne migrierende Partialepilepsie des Kindes Monogene Krankheit mit Epilepsie Familiäre fokale Epilepsie mit variablen Herden W-Syndrom Zerebrale Fehlbildung mit Epilepsie Akute Enzephalopathie mit entzündungsvermitteltem Status Epilepticus Epilepsie mit frühem Beginn-Intelligenzminderung-Gehirnanomalien-Syndrom Familiäres Epilepsiesyndrom, idiopathisches oder kryptogenes, mit bekanntem Gen/-ort Stoffwechselstörung mit Epilepsie Inflammatorische und autoimmune Krankheit mit Epilepsie Infektionskrankheit mit Epilepsie Temporallappenepilepsie, mesiale, mit Fieberkrämpfen, familiäre Form Zerebrale Gefäßkrankheiten mit Epilepsie Zöliakie-Epilepsie-zerebrale Verkalkungen-Syndrom Epileptische Enzephalopathie mit globaler zerebraler Demyelinisierung 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 Myoclonic-astatic epilepsy Benign idiopathic neonatal seizures Early-onset progressive encephalopathy with migrant continuous myoclonus Myoclonic epilepsy in non-progressive encephalopathies Benign familial infantile epilepsy Juvenile myoclonic epilepsy Rolandic epilepsy Benign familial neonatal-infantile seizures Infantile spasms-broad thumbs syndrome KCNQ2-related epileptic encephalopathy Familial partial epilepsy Autosomal dominant nocturnal frontal lobe epilepsy Childhood absence epilepsy Benign partial epilepsy with secondarily generalized seizures in infancy Epilepsy-microcephaly-skeletal dysplasia syndrome Infantile epileptic-dyskinetic encephalopathy Benign familial neonatal epilepsy Infantile spasms syndrome Benign partial epilepsy of infancy with complex partial seizures Epilepsy-telangiectasia syndrome Continuous spikes and waves during sleep CDKL5-deficiency disorder Benign focal seizures of adolescence Benign partial infantile seizures Benign familial mesial temporal lobe epilepsy X-linked epilepsy-learning disabilities-behavior disorders syndrome Benign occipital epilepsy Infantile epilepsy syndrome Neonatal epilepsy syndrome Adolescent-onset epilepsy syndrome Dravet syndrome Benign childhood occipital epilepsy, Panayiotopoulos type Epilepsy syndrome Infantile convulsions and choreoathetosis Paroxysmal dyskinesia