Show Summary Details

Page of

PRINTED FROM OXFORD HANDBOOKS ONLINE ( © Oxford University Press, 2018. All Rights Reserved. Under the terms of the licence agreement, an individual user may print out a PDF of a single chapter of a title in Oxford Handbooks Online for personal use (for details see Privacy Policy and Legal Notice).

date: 27 January 2021

Abstract and Keywords

Genetic factors are believed to account for more than half of all cases of congenital or early-onset moderate to profound deafness. The identification of several dozen genes for deafness, one of which accounts for a high proportion of all childhood deafness, has enabled the identification of the exact cause of deafness in many children through genetic testing. Parents, family members, deaf and hard-of-hearing adults, as well as health care and educational professionals often are unaware of the exact process and goals of genetic evaluation and may have questions about the usefulness of genetic testing. Sensitive and appropriate genetic evaluation and testing, coupled with appropriate interpretation and information through genetic counseling, can be invaluable to many families. Health professionals and those who work with deaf children in educational and service settings play an important role in helping parents and family members understand the value of a genetic evaluation and making referrals to genetics professionals.

Keywords: genetics, autosomal dominant, autosomal recessive, connexin 26, deaf, hard-of-hearing, hearing loss

Access to the complete content on Oxford Handbooks Online requires a subscription or purchase. Public users are able to search the site and view the abstracts and keywords for each book and chapter without a subscription.

Please subscribe or login to access full text content.

If you have purchased a print title that contains an access token, please see the token for information about how to register your code.

For questions on access or troubleshooting, please check our FAQs, and if you can''t find the answer there, please contact us.