PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0014544|epilepsies |
| Sentences | 5 |
| PubMedID- 24260362 | Thirteen patients (age mean of years; 8 females; mean duration of epilepsy years) with pharmacoresistant epilepsies of suspected temporal or extratemporal neocortical origin as well as twenty healthy controls (age mean of years; 10 females) were included in the study. |
| PubMedID- 23418441 | It is also important to identify the types and etiologies of epilepsies associated with maternal epilepsy, the use of art as well as short umbilical cord length. |
| PubMedID- 21903728 | There was a significant difference in the braak stages between epilepsy syndrome diagnoses, with partial epilepsies (including temporal lobe epilepsy) more often associated with higher braak stages than genetic or idiopathic generalized epilepsies.table 2epilepsy syndrome and braak staging in 138 casesepilepsy syndrome classification and aetiologysyndromenumber of cases (of 138)braak stages (% cases)0iiiiiiivvpartial/focal/structuralpartial epilepsy6617.712.92916.124.20temporal lobe epilepsy1643.8037.506.212.5post-traumatic epilepsya333.30033.333.30genetic/idiopathicidiopathic generalized728.642.9014.314.30dravet syndrome333670000progressive myoclonic epilepsy101000000unknownsyndrome classification not possible4643.517.410.910.915.22.2a post-traumatic epilepsy has been included as a separate category for the purposes of this study. |
| PubMedID- 22957247 | Similar to other focal onset epilepsies, children with temporal lobe epilepsy are often initially treated through medication management. |
| PubMedID- 25923336 | 22 patients were selected with primary diagnosis of different types of epilepsies including epilepsy (epi), epilepsy plus mental retardation (epi+mr) and juvenile myoclonic epilepsy (jme) shown in the table 1. details of all patients are as follows; case 1190 and 1193: 1193 is a 4 years old female proband; her seizures were started at the age of 3 years. |
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