PedAM
Pediatric Disease Annotations & Medicines
| Disease | epilepsy |
| Phenotype | C0013384|dyskinesia |
| Sentences | 2 |
| PubMedID- 23776372 | Deleterious dominant mutations cause glucose transporter type 1 (glut1) deficiency leading to paroxysmal exertional dyskinesia together with epilepsy and intellectual disability in family members. |
| PubMedID- 26132164 | An association of familial rolandic epilepsy with exercise-induced dyskinesia and dystonic writer’s cramp has been reported [26], but no causative gene has been found. |
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