episodic ataxia type 6

Episodic ataxia type 6 (EA6) is an exceedingly rare form of hereditary episodic ataxia with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia.

Also known as: SLC1A3 hereditary episodic ataxia, hereditary episodic ataxia caused by mutation in SLC1A3, EA6, episodic ataxia, type 6

Category: General

What is episodic ataxia type 6?

episodic ataxia type 6 is a recognized medical condition. This page explains what it is, symptoms that may accompany it, and the lab tests healthcare providers sometimes use to investigate it. It is educational information only and is not a diagnosis.

If you think you may have episodic ataxia type 6, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with episodic ataxia type 6

DiplopiaHemiparesisMigraineNauseaSeizureVertigoVomiting

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.