About External auditory canal aplasia/hypoplasia
External auditory canal aplasia/hypoplasia is a rare disease catalogued by Orphanet (ORPHA:141074). It is associated with the TSHZ1 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 External auditory canal aplasia/hypoplasia trials.
Search ClinicalTrials.gov for "External auditory canal aplasia/hypoplasia" or filter by Orphanet code ORPHA:141074 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
Find recruiting External auditory canal aplasia/hypoplasia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for External auditory canal aplasia/hypoplasia. Updated daily.