Catalog

Episodic ataxia type 5 - CACNB4 mutation

No MMS code

Link to WHO Definition

Episodic ataxia type 5 - CACNB4 mutation – http://id.who.int/icd/entity/2072072482

Episodic ataxia type 5 (EA5) is an extremely rare form of Hereditary episodic ataxia characterised by recurrent episodes of vertigo and ataxia lasting several hours.