This website provides information on patients with mutations in the ATOH1 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the ATOH1 gene is a multisystem disorder characterized by progressive hearing loss of congenital or early childhood onset, mostly mild-moderate severity

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the ATOH1 gene.

Karen B. Avraham, PhD, Tel Aviv University, Tel Aviv, Israel, karena@tauex.tau.ac.il

Zippora Brownstein, PhD, Tel Aviv University, Tel Aviv, Israel, brownste@tauex.tau.ac.il