eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | dystonia |
| Comorbidity | 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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