Genetics of non syndromic hearing loss

M. D. Venkatesh, Nikhil Moorchung, Bipin Puri

Research output: Contribution to journalReview articlepeer-review

20 Citations (Scopus)


Non Syndromic Hearing Loss is an important cause for hearing loss. One in 1000 newborns have some hearing impairment. Over 400 genetic syndromes have been described. Non Syndromic Hearing Loss (NSHL) can be inherited in an Autosomal Dominant, Autosomal Recessive or a Sex Linked fashion. There are several reasons why genetic testing should be done in cases of NSHL, the main reasons being for genetic screening and for planning treatment. This review describes the genes involved in NSHL and the genetic mechanisms involved in the pathogenesis of the disease.

Original languageEnglish
Pages (from-to)363-368
Number of pages6
JournalMedical Journal Armed Forces India
Issue number4
Publication statusPublished - 10-2015

All Science Journal Classification (ASJC) codes

  • Medicine(all)


Dive into the research topics of 'Genetics of non syndromic hearing loss'. Together they form a unique fingerprint.

Cite this