Table 3.
Epilepsy and epileptic syndromes | Number |
---|---|
Ohtahara syndrome | 1 |
Hypoxic ischemic encephalopathy | |
West syndrome | 21a |
2 hypoxic ischemic encephalopathies 5 chromosomal anomaly or syndrome 3 tuberous sclerosis complex | |
5 structural anomalies | |
1 perinatal insult and 1 congenital hyperinsulinism 5 unknown etiologies | |
Myoclonic epilepsy of infancy | 1 |
Genetic febrile seizures plus | 1 |
Epilepsy with myoclonic atonic seizures | 1 |
Eyelid myoclonia | 1 |
Epileptic encephalopathy with continuous spikes and waves during sleep | 2 |
1 unknown etiology and 1 chromosomal anomaly | |
Landau‐Kleffner syndrome | 1 |
Gelastic seizures with hypothalamic hamartoma | 1 |
Epilepsy with malformations of cortical and brain development | 16 |
3 focal cortical dysplasias 1 schizencephalia | |
3 porencephalia/holoprosencephalies | |
9 corpus callosum hypoplasia/aplasias or other structural anomalies | |
Epilepsy with tumor | 1 |
1 Glioma | 1 |
Epilepsy with infection | 4 |
2 congenital infections | |
1 meningitis and 1 encephalitis | |
Epilepsy with trauma | 2 |
1 traumatic brain injury and 1 near‐drowning | |
Epilepsy with perinatal insult | 15 |
2 birth asphyxias | |
5 hypoxic ischemic encephalopathies 1 cerebral infarction | |
7 cases of intracerebral bleeding | |
Epilepsy with stroke | 1 |
1 case of cerebral bleeding | |
Epilepsy with metabolic reason | 4b |
2 cases of congenital hyperinsulinism | |
1 Glut1‐deficiency syndrome and 1 3‐methylglutaric aciduria | |
Epilepsy with chromosomal anomalies and syndromes | 17c |
5 chromosomal anomalies | |
3 Catch syndromes | |
2 fragile‐X syndromes | |
1 Peho syndrome | |
1 Angelmann syndrome and 1 Aicardi syndrome 1 Rett syndrome and 1 Masa syndrome | |
1 Coats syndrome and 1 Sotos syndrome | |
Focal epilepsy and developmental delay | 8 |
Generalized epilepsy and developmental delay | 2 |
Unclassified epilepsy and epilepsy of unknown etiology | 1 |
Total | 101 |
Of all the children with epilepsy, cognitive impairment was seen in 101 out of 289, or 35%.
The West syndrome group includes patients from other groups such as those with epilepsy with malformation in cortical and brain development, chromosomal anomalies and syndromes, perinatal insult, and metabolic reasons.
The West syndrome group includes one congenital‐hyperinsulinism patient.
The West syndrome group includes one Peho‐syndrome patient.