From: Etiological analysis of 167 cases of drug-resistant epilepsy in children
Clinical manifestations | Patients, No.(%) |
---|---|
Epilepsy syndromes | 60 (35.9) |
Epilepsy syndromes with onset in neonates and infants | 36 (60) |
āInfantile epileptic spasm syndrome (IESS) | 14 |
āDravet syndromes | 6 |
āEtiology specific epileptic encephalopathy | 4 |
āEarly-infantile DEE (EIDEE) | 2 |
āLennox-Gastaut syndrome | 1 |
āHard to classification of epilepsy syndrome | 9 |
epilepsy syndromes with onset in childhood | 24 (40) |
āDevelopmental and/or epileptic encephalopathies (DEEs) | 17 |
ā āLennox-Gastaut syndrome | 4 |
ā āFebrile infection-related epilepsy syndrome,FIRES | 2 |
ā āHemiconvulsionāhemiplegiaāepilepsy syndrome, HHE | 1 |
ā āHard to classification of epilepsy syndrome | 10 |
āSelf-limited focal epilepsies (SeLFEs) | 7 |
Others | 107 (64.1) |
Focal seizures | 53 (49.5) |
Generalized seizures | 16(14.9) |
āGeneralized tonic-clonic seizure,GTCS | 11 |
āAbsence seizures | 3 |
āClonic seizures | 1 |
āMyoclonic seizures | 1 |
Multiple seizure types | 40(37.3) |