Disease Directory Duane retraction syndrome with congenital deafness
Rare Disease

Duane retraction syndrome with congenital deafness

Type

Malformation syndrome

Gene

MAFB

About Duane retraction syndrome with congenital deafness

Duane retraction syndrome with congenital deafness is a rare disease catalogued by Orphanet (ORPHA:529574). It is associated with the MAFB gene. 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.

Clinical Trial Eligibility Tips

What to know before applying to Duane retraction syndrome with congenital deafness trials.

Search ClinicalTrials.gov for "Duane retraction syndrome with congenital deafness" or filter by Orphanet code ORPHA:529574 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

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

Patient Resources

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:529574)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Duane retraction syndrome with congenital deafness trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Duane retraction syndrome with congenital deafness. Updated daily.