Focal |
Self-limited neonatal epilepsy (SeLNE) |
Self-limited familial neonatal and infantile epilepsy (SeLFNIE) |
Self-limited infantile epilepsy (SeLIE) |
Focal and/or generalized |
Genetic epilepsy with febrile seizures plus (GEFS+) |
Generalized |
Myoclonic epilepsy in infancy (MEI) |
Developmental and epileptic encephalopathies (DEEs) |
Early infantile DEE (EIDEE) |
Epilepsy in infancy with migrating focal seizures (EIMFS) |
Infantile epileptic spasms syndrome (IESS) |
Dravet syndrome (DS) |
Etiology-specific syndromes* |
KCNQ2 DEE (KCNQ2-DEE) |
Pyridoxine-dependent (ALDH7A1) DEE (PD-DEE) |
Pyridoxamine 5'-phosphate deficiency (PNPO) DEE (P5PD-DEE) |
CDKL5 DEE (CDKL5-DEE) |
Protocadherin 19 clustering epilepsy (PCDH19 clustering epilepsy) |
Glucose transporter 1 deficiency syndrome (GLUT1DS) |
Sturge-Weber syndrome (SWS) |
Gelastic seizures with hypothalamic hamartoma (GS-HH) |
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