Catalog

Episodic ataxia type 2 - CACNA1A mutation

No MMS code

Link to WHO Definition

Episodic ataxia type 2 - CACNA1A mutation – http://id.who.int/icd/entity/1470995662

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.