Episodic ataxia type 1 - KCNA1 mutation (Q90146): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Ataxia episódica tipo 1 é uma forma frequente de ataxia episódica hereditária, caracterizada por breves episódios de ataxia, neuromiotonia e mioquimia interictal contínua. Algumas vezes responde a acetalozamida. | |||
| description / en | description / en | ||
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. | |||
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 |
||
| 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. |
