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Benign paroxysmal tonic upgaze of childhood with ataxia

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Just diagnosed with Benign paroxysmal tonic upgaze of childhood with ataxia?

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Overview

Benign paroxysmal tonic upgaze of childhood with ataxia is a rare condition. Also known as Ouvrier-Billson syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Benign paroxysmal tonic upgaze of childhood with ataxia so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1179 · OMIM 168885 · ICD-10 G96.8 · GARD 0004176

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Authoritative references for Benign paroxysmal tonic upgaze of childhood with ataxia

Research & market landscape for Benign paroxysmal tonic upgaze of childhood with ataxia

Following Benign paroxysmal tonic upgaze of childhood with ataxia for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Benign paroxysmal tonic upgaze of childhood with ataxia — the real-world landscape behind the condition, in one place.

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Common questions

What is Benign paroxysmal tonic upgaze of childhood with ataxia?

Benign paroxysmal tonic upgaze of childhood with ataxia is a rare condition. Also known as Ouvrier-Billson syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Benign paroxysmal tonic upgaze of childhood with ataxia together in one place.

What are the symptoms of Benign paroxysmal tonic upgaze of childhood with ataxia?

Symptoms of Benign paroxysmal tonic upgaze of childhood with ataxia 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 Benign paroxysmal tonic upgaze of childhood with ataxia.

How is Benign paroxysmal tonic upgaze of childhood with ataxia treated?

Treatment for Benign paroxysmal tonic upgaze of childhood with ataxia depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Benign paroxysmal tonic upgaze of childhood with ataxia, and review current options with them.

What causes Benign paroxysmal tonic upgaze of childhood with ataxia — is it genetic?

The cause and inheritance of Benign paroxysmal tonic upgaze of childhood with ataxia are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Benign paroxysmal tonic upgaze of childhood with ataxia can explain what it means for you and your family.

I was just diagnosed with Benign paroxysmal tonic upgaze of childhood with ataxia — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Benign paroxysmal tonic upgaze of childhood with ataxia, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Benign paroxysmal tonic upgaze of childhood with ataxia?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Benign paroxysmal tonic upgaze of childhood with ataxia, filtered to your area.

Are there clinical trials for Benign paroxysmal tonic upgaze of childhood with ataxia?

Tomeko shows live, recruiting studies for Benign paroxysmal tonic upgaze of childhood with ataxia from ClinicalTrials.gov on the hub.

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