Autosomal dominant nonsyndromic deafness 10: Symptoms, Diagnosis and Treatment

By Dr. Karen Robinson, MD · 2021-04-24 · Neurology

This article from Weyland-Yutani Health System's Neurology service line explains autosomal dominant nonsyndromic deafness 10 in plain language.

About this topic

Topic: autosomal dominant nonsyndromic deafness 10. An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.

Mentioned in this article

• child neurologist evaluation

Related care

• nucleoside and nucleotide reverse transcriptase inhibitor therapy

Always talk with your care team before making decisions about your health. This content is educational only.