Status: Recruiting
Otoferlin Patient Registry and Natural History Study
This registry is designed to collect comprehensive information about the molecular genetic diagnoses of individuals with otoferlin-associated hearing impairment and clinical information to support a natural history study.
Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: Tobias MoserUpdated: May 28, 2025Locations: 1Duration: 25 Years
Eligibility criteria
A molecular genetic diagnosis involving biallelic variants in otoferlin (OTOF) a...
Patients with evidence of non-OTOF molecular genetic diagnoses