Version May 2024
| Syndrome group | Syndrome name | Abbreviation |
| Neonatal-infant | CDKL5-developmental and epileptic encephalopathy | CDKL5-DEE |
| Dravet syndrome | DS | |
| Early infantile developmental and epileptic encephalopathy | EIDEE | |
| Epilepsy of infancy with migrating focal seizures | EIMFS | |
| Genetic epilepsy with febrile seizures plus | GEFS+ | |
| Gelastic seizures with hypothalamic hamartoma | GS-HH | |
| Glucose transporter 1 deficiency syndrome | GLUT1DS | |
| Infantile epileptic spasm syndrome | IESS | |
| KCNQ2-developmental and epileptic encephalopathy | KCNQ2-DEE | |
| Myoclonic epilepsy in infancy | MEI | |
| Protocadherin 19 clustering epilepsy | PCDH19 clustering epilepsy | |
| Pyridoxine-dependent (ALDH7A1) developmental and epileptic encephalopathy | PD-DEE | |
| Pyridox(am)ine 5'-phosphate deficiency (PNPO) developmental and epileptic encephalopathy | P5PD-DEE | |
| Self-limited familial neonatal-infantile epilepsy | SeLFNIE | |
| Self-limited infantile epilepsy | SeLIE | |
| Self-limited neonatal epilepsy | SeLNE | |
| Sturge-Weber syndrome | SWS | |
| Child | Childhood occipital visual epilepsy | COVE |
| Developmental and epileptic encephalopathy with spike-and-wave activation in sleep | DEE-SWAS | |
| Epileptic encephalopathy with spike-and-wave activation in sleep | EE-SWAS | |
| Epilepsy with eyelid myoclonia | EEM | |
| Epilepsy with myoclonic absences | EMA | |
| Epilepsy with myoclonic-atonic seizures | EMAtS | |
| Febrile infection-related epilepsy syndrome | FIRES | |
| Hemiconvulsion-hemiplegia epilepsy syndrome | HHE | |
| Lennox-Gastaut syndrome | LGS | |
| Photosensitive occipital lobe epilepsy | POLE | |
| Self-limited epilepsy with autonomic seizures | SeLEAS | |
| Self-limited epilepsy with centrotemporal spikes | SeLECTS | |
| Idiopathic generalized epilepsies | Childhood absence epilepsy | CAE |
| Epilepsy with generalized tonic-clonic seizures alone | GTCA | |
| Juvenile absence epilepsy | JAE | |
| Juvenile myoclonic epilepsy | JME | |
| Variable age | Epilepsy with auditory features | EAF |
| Epilepsy with reading-induced seizures | EwRIS | |
| Familial focal epilepsy with variable foci | FFEVF | |
| Familial mesial temporal lobe epilepsy | FMTLE | |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | MTLE-HS | |
| Progressive myoclonus epilepsies | PME | |
| Rasmussen syndrome | RS | |
| Sleep-related hypermotor (hyperkinetic) epilepsy | SHE |
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