Status: Recruiting
CABP2 Patient Registry and Natural History Study
This registry is designed to collect comprehensive information about the molecular genetic diagnoses and clinical information of individuals with CABP2-associated hearing impairment to support a natural history study.
Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: University Medical Center GoettingenUpdated: Jan 27, 2026Locations: 1Duration: 25 Years
Eligibility criteria
A molecular genetic diagnosis involving biallelic variants in CAPB2 and audiomet...
Patients with evidence of non-CABP2 molecular genetic diagnoses