Clinical Trial: A Natural History Study in Pediatric Participants With Hearing Loss Due to OTOF, GJB2, or GJB2/GJB6 Mutations
Study Status: Completed
Recruit Status: RECRUITING
Condition: Congenital Hearing Loss Secondary to Biallelic Mutations in the Otoferlin Gene (OTOF)
Study Type: OBSERVATIONAL
Official Title: A Retrospective and Prospective Natural History Study to Examine the Characteristics of Gene-Related Hearing Loss in Pediatric Participants With Biallelic Otoferlin (OTOF) Mutations, Gap Junction Beta
Brief Summary:
This is an observational study to examine the characteristics of gene-related hearing loss in pediatric participants with biallelic otoferlin (OTOF) Mutations, Gap Junction Beta 2 (GJB2) Mutations, or Digenic GJB2/Gap Junction Beta 6 (GJB6) Mutations.This study will follow the participant for 4 years with annual visits each year.
Read more