SE-ATLAS

SYNGAP1-related developmental and epileptic encephalopathy Distal duplication 15q Inverted duplicated chromosome 15 syndrome Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression Severe neonatal-onset encephalopathy with microcephaly Familial infantile myoclonic epilepsy Progressive myoclonic epilepsy with dystonia Sturge-Weber syndrome Idiopathic hemiconvulsion-hemiplegia syndrome Myoclonic epilepsy of infancy Benign non-familial infantile seizures Benign familial neonatal-infantile seizures Benign familial infantile epilepsy Myoclonic epilepsy in non-progressive encephalopathies Early-onset progressive encephalopathy with migrant continuous myoclonus Benign partial epilepsy of infancy with complex partial seizures Infantile spasms syndrome Benign infantile seizures associated with mild gastroenteritis Benign partial epilepsy with secondarily generalized seizures in infancy Benign infantile focal epilepsy with midline spikes and waves during sleep Angelman syndrome due to paternal uniparental disomy of chromosome 15 Angelman syndrome due to maternal 15q11q13 deletion Benign partial infantile seizures Infantile epilepsy syndrome Dravet syndrome Lennox-Gastaut syndrome Infantile convulsions and choreoathetosis Angelman syndrome Atypical Rett syndrome Generalized epilepsy with febrile seizures-plus STXBP1-related encephalopathy