Epilepsy syndromes are characterized by various severities, from relatively mild febrile seizures and generalized epilepsy with febrile seizures plus (FEB3A, generalized epilepsy with febrile seizures plus type 2; GEFSP2/GEFS+, OMIM 604403) to severe forms of DEE, such as the Dravet syndrome (DRVT; OMIM 607208) or developmental and epileptic encephalopathy 6B, non-Dravet (DEE6B; OMIM 619317). The gene discussed is SCN1A; the disease is idiopathic generalized epilepsy.