Disease Directory Benign paroxysmal tonic upgaze of childhood with ataxia
Neurological

Benign paroxysmal tonic upgaze of childhood with ataxia

Type

Disease

About Benign paroxysmal tonic upgaze of childhood with ataxia

Benign paroxysmal tonic upgaze of childhood with ataxia is a rare disease catalogued by Orphanet (ORPHA:1179). Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries worldwide.

Clinical Trial Eligibility Tips

What to know before applying to Benign paroxysmal tonic upgaze of childhood with ataxia trials.

Search ClinicalTrials.gov for "Benign paroxysmal tonic upgaze of childhood with ataxia" or Orphanet code ORPHA:1179 to find disease-specific recruiting studies.

Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.

Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:1179)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Benign paroxysmal tonic upgaze of childhood with ataxia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Benign paroxysmal tonic upgaze of childhood with ataxia. Updated daily.