Episodic ataxia type 1 - KCNA1 mutation (Q90146): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_2135559917 | |||
| Property / CURIE: CID11:ID_2135559917 / rank | |||
Normal rank | |||
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. |
Statements
CID11:ID_2135559917
0 references
