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Episodic ataxia type 3

Specialists and centers, recruiting clinical trials, patient organizations, research, and community for Episodic ataxia type 3 — brought together in one place.

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Just diagnosed with Episodic ataxia type 3?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Episodic ataxia type 3, look for clinical trials, and connect with others living with it — all in one place.

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Overview

Episodic ataxia type 3 is a rare condition. Also known as Episodic ataxia-vertigo-tinnitus-myokymia syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Episodic ataxia type 3 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:79135 · OMIM 606554 · ICD-10 G11.8 · GARD 0016702

Find care for Episodic ataxia type 3

Authoritative references for Episodic ataxia type 3

Research & market landscape for Episodic ataxia type 3

Following Episodic ataxia type 3 for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Episodic ataxia type 3 — the real-world landscape behind the condition, in one place.

Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Episodic ataxia type 3 and every rare condition. See how Tomeko works with industry →

Common questions

What is Episodic ataxia type 3?

Episodic ataxia type 3 is a rare condition. Also known as Episodic ataxia-vertigo-tinnitus-myokymia syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Episodic ataxia type 3 together in one place.

What are the symptoms of Episodic ataxia type 3?

Symptoms of Episodic ataxia type 3 vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Episodic ataxia type 3.

How is Episodic ataxia type 3 treated?

Treatment for Episodic ataxia type 3 depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Episodic ataxia type 3, and review current options with them.

What causes Episodic ataxia type 3 — is it genetic?

The cause and inheritance of Episodic ataxia type 3 are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Episodic ataxia type 3 can explain what it means for you and your family.

I was just diagnosed with Episodic ataxia type 3 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Episodic ataxia type 3, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Episodic ataxia type 3?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Episodic ataxia type 3, filtered to your area.

Are there clinical trials for Episodic ataxia type 3?

Tomeko shows live, recruiting studies for Episodic ataxia type 3 from ClinicalTrials.gov on the hub.

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