SE-ATLAS

Childhood disintegrative disorder Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Neurocutaneous syndrome with epilepsy Landau-Kleffner syndrome Monogenic disease with epilepsy Cerebral malformation with epilepsy Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Metabolic diseases with epilepsy Acute encephalopathy with inflammation-mediated status epilepticus Atypical autism Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Cerebral diseases of vascular origin with epilepsy Atypical Rett syndrome Rett syndrome Generalized epilepsy with febrile seizures-plus Non-specific early-onset epileptic encephalopathy Rare epilepsy Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Muscular channelopathy Skeletal muscle disease Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Familial infantile myoclonic epilepsy Neuromuscular junction disease Idiopathic hemiconvulsion-hemiplegia syndrome Progressive myoclonic epilepsy with dystonia Myoclonic epilepsy of infancy Motor neuron disease Epilepsy with myoclonic absences Myoclonic-astatic epilepsy Myoclonic epilepsy in non-progressive encephalopathies Early-onset progressive encephalopathy with migrant continuous myoclonus Perioral myoclonia with absences Familial partial epilepsy Reflex epilepsy Cryptogenic late-onset epileptic spasms Infantile spasms syndrome Epilepsy with eyelid myoclonia Continuous spikes and waves during sleep Neuromuscular disease Benign partial infantile seizures Juvenile myasthenia gravis Neurometabolic disease Rare developmental defect during embryogenesis Rare disease with autism Benign occipital epilepsy Rolandic epilepsy-speech dyspraxia syndrome Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Childhood-onset epilepsy syndrome Infantile epilepsy syndrome Neonatal epilepsy syndrome Progressive myoclonic epilepsy Rare pervasive developmental disorder Dravet syndrome Lennox-Gastaut syndrome