Episodic ataxia type 2 - CACNA1A mutation (Q90142): Difference between revisions
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Ataxia paroxística familiar é uma forma de ataxia cerebelar caracterizada por episódios agudos de ataxia, vertigem e náuseas, com duração variando de poucos minutos a muitas horas. Os episódios podem ser acompanhados por disartria, diplopia, distonia ou hemiplegia. | |||
| description / en | description / en | ||
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. | |||
Revision as of 17:05, 15 August 2026
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 |
|---|---|---|---|
| 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. |
