Table 1.
Genetic, N = 91 (32%) | |
Genetic | |
Chromosomal or gene abnormalities | 20 |
Presumed genetic | |
Epileptic encephalopathy | 5 |
Generalized genetic epilepsies | 39 |
Focal genetic epilepsy | 27 |
Structural, N = 84 (29%) | |
Malformation of cortical and brain development | 29 |
Hypothalamic hamartoma | 1 |
Tuberous sclerosis | 3 |
Vascular malformation | 2 |
Trauma | 7 |
Perinatal insult | 35 |
Stroke | 1 |
Tumor | 5 |
Angioma | 1 |
Metabolic, N = 4 (1%) | |
Congenital hyperinsulinism | 3 |
3‐methylglutaricaciduria | 1 |
Infection, N = 9 (3%) | |
Congenital infection | 2 |
Encephalitis | 4 |
Meningitis | 2 |
Unspecified | 1 |
Immunological, N = 0 (0%) | 0 |
Unknown, N = 101 (35%) | 101 |