The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Book Review
PreviousPrevious
Volume 333:1090-1091 October 19, 1995 Number 16
NextNext

Hereditary Hearing Loss and Its Syndromes

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

 Sign up for free e-toc
 

This Article
-Full Text
-Purchase this article

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited

More Information
(Oxford Monographs on Medical Genetics. No. 28.) Edited by Robert J. Gorlin, Helga V. Toriello, and M. Michael Cohen, Jr. 457 pp., illustrated. New York, Oxford University Press, 1995. $195. ISBN 0-19-506552-2

Hearing loss is perhaps the most prevalent of all the chronic diseases, with over 20 million Americans suffering from hearing impairment severe enough to affect their ability to communicate. The profound deafness that affects roughly 1 in 1000 newborns has obvious implications in terms of early-childhood education, parental adjustments to the use of manual communication, and the social isolation that may ensue. During the past decade there has been a tremendously exciting explosion of basic- and clinical-research findings in the area of mammalian hearing loss. This has resulted in part from increased attention to the importance of communication disorders in . . . [Full Text of this Article]




HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.