Living With Autosomal dominant nonsyndromic deafness 3A

By Dr. Aaliyah Ortiz, MD · 2022-07-16 · Neurology

This article from Weyland-Yutani Health System's Neurology service line explains autosomal dominant nonsyndromic deafness 3A in plain language.

About this topic

Topic: autosomal dominant nonsyndromic deafness 3A. An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.

Mentioned in this article

• T cell morphology measurement

Related care

• pain management for palliative care
• cerebrospinal fluid specimen collection

This article is for general information and does not replace advice from your clinician.