Episodic ataxia type 1 - KCNA1 mutation (Q90146): Difference between revisions
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Latest revision as of 17:05, 15 August 2026
Episodic ataxia type 1 is a frequent form of hereditary episodic ataxia, characterized by brief episodes of ataxia, neuromyotonia, and continuous interictal myokymia. It sometimes responds to acetazolamide.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2135559917 |
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| English | Episodic ataxia type 1 - KCNA1 mutation |
Episodic ataxia type 1 is a frequent form of hereditary episodic ataxia, characterized by brief episodes of ataxia, neuromyotonia, and continuous interictal myokymia. It sometimes responds to acetazolamide. |
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CID11:ID_2135559917
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dki-india-ID_2135559917
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Concluído
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13 August 2026
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