SE-ATLAS

Chromosomal anomaly with epilepsy as a major feature Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy Cerebral malformation with epilepsy Rare epilepsy Benign familial infantile epilepsy Cystic fibrosis Rare sucking/swallowing disorder Infantile epilepsy syndrome Childhood-onset epilepsy syndrome Neurocutaneous syndrome with epilepsy Epilepsy syndrome