PedAM
Pediatric Disease Annotations & Medicines
| Disease | dystonia |
| Phenotype | C0014553|absence epilepsy |
| Sentences | 2 |
| PubMedID- 20213496 | The tottering phenotype, an autosomal recessive mouse disease, is associated with mild ataxia, spontaneous behavioral arrest associated with synchronous, bilateral cortical polyspike discharges (resembling human absence epilepsy), and attacks of paroxysmal dystonia [10, 61]. |
| PubMedID- 26132164 | Dysgraphia as a mild expression of dystonia in children with absence epilepsy. |
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