Episodic ataxia type 2 - CACNA1A mutation (Q90142)
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Familial paroxysmal ataxia is a form of cerebellar ataxia characterised by episodes of acute ataxia, dizziness and nausea, with a duration ranging from a few minutes to several hours. The episodes may be accompanied by dysarthria, diplopia, dystonia or hemiplegia.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1470995662 |
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| English | Episodic ataxia type 2 - CACNA1A mutation |
Familial paroxysmal ataxia is a form of cerebellar ataxia characterised by episodes of acute ataxia, dizziness and nausea, with a duration ranging from a few minutes to several hours. The episodes may be accompanied by dysarthria, diplopia, dystonia or hemiplegia. |
