SE-ATLAS

Neurocutaneous syndrome with epilepsy Chromosomal anomaly with epilepsy as a major feature Angelman syndrome Monogenic disease with epilepsy Cerebral malformation with epilepsy Neonatal epilepsy syndrome Childhood-onset epilepsy syndrome Infantile epilepsy syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Early infantile epileptic encephalopathy Metabolic diseases with epilepsy Adolescent-onset epilepsy syndrome Angelman syndrome due to paternal uniparental disomy of chromosome 15 Dravet syndrome Tuberous sclerosis complex Angelman syndrome due to maternal 15q11q13 deletion Rare epilepsy Familial partial epilepsy Infantile spasms syndrome Epilepsy syndrome Angelman syndrome due to a point mutation Benign familial infantile epilepsy Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gorlin syndrome Angelman syndrome due to imprinting defect in 15q11-q13 Benign familial neonatal-infantile seizures