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 spasms 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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