SE-ATLAS

Non-herpetic acute limbic encephalitis Chromosomal anomaly with epilepsy as a major feature Limbic encephalitis with LGI1 antibodies Limbic encephalitis with nCMAgs antibodies Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy Limbic encephalitis with neurexin-3 antibodies Non-paraneoplastic limbic encephalitis Paraneoplastic limbic encephalitis NMDA receptor encephalitis Cerebral malformation with epilepsy Hyperekplexia Posttransplant acute limbic encephalitis Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Rare epilepsy Dravet syndrome Isaacs syndrome Limbic encephalitis with caspr2 antibodies Bickerstaff brainstem encephalitis Limbic encephalitis with DPP6 antibodies Limbic encephalitis Classic paraneoplastic limbic encephalitis Progressive encephalomyelitis with rigidity and myoclonus Limbic encephalitis associated with antibodies to cell membrane antigens Acute disseminated encephalomyelitis Epilepsy syndrome Neurocutaneous syndrome with epilepsy Morvan syndrome Non-specific early-onset epileptic encephalopathy Febrile infection-related epilepsy syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Pyridoxal phosphate-responsive seizures ARX-related epileptic encephalopathy Epileptic encephalopathy with global cerebral demyelination KCNQ2-related epileptic encephalopathy CDKL5-deficiency disorder Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome Continuous spikes and waves during sleep Lethal neonatal spasticity-epileptic encephalopathy syndrome Tuberous sclerosis complex Hypothalamic hamartomas with gelastic seizures Early infantile epileptic encephalopathy