Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes
Conditions
Sensorineural Hearing Loss, Bilateral · AUNB1 · DFNB1A · Congenital Deafness · DFNB9 · OTOF Gene Mutation · GJB2 Gene Mutation
Simple summaryAI-assisted
This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.
Locations
Necker Hospital, Paris, France
Study leads
Natalie LOUNDON, MD
Principal Investigator
Necker Hospital