Episodic Ataxia, Type 2 Community

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Community Members: 3

Brief Description

Episodic Ataxia, Type 2 is a rare genetic disorder characterized by sporadic episodes of severe discoordination caused by mutations in CACNA1A.

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Synonyms

Type 2 episodic ataxia, EA2, episodic ataxia with nystagmus, hereditary paroxysmal cerebellopathy, familial paroxysmal ataxia and acetazolamide-responsive hereditary paroxysmal cerebellar ataxia (AHPCA)

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Community Members

1. 

   nairb

   

   jory

   

   dizzyblonde