eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | episodic ataxia |
| Comorbidity | C0007760|cerebellar dysfunction |
| Sentences | 1 |
| PubMedID- 25642194 | episodic ataxia type 1 (ea1) is an autosomal dominant k+ channelopathy which manifests as brief episodes of cerebellar dysfunction with paroxysmal ataxia, dysarthria, diplopia, vertigo and tremor often lasting for seconds or minutes. |
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