Episodic ataxia type 1 - KCNA1 mutation (Q90146)
From determinar.ia.br - Determine suas informações
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 |
||
| 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. |
