Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 2 of 2 for Profound sensorineural hearing impairment
  1. STRC gene 
    ... gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet A. 2012 Feb;158A( ... T. DFNB16 is a frequent cause of congenital hearing impairment: implementation ... RJ. Sensorineural deafness and male infertility: a contiguous gene deletion ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  2. TECTA gene 
    ... are mutated in each cell. This form of hearing loss is usually severe to profound and is prelingual.The TECTA gene mutations that ... results in autosomal dominant, postlingual, progressive, mid frequency hearing ... form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics