Semin Hear 2007; 28(3): 216-225
DOI: 10.1055/s-2007-982903
Copyright © 2007 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Genetics, Hereditary Hearing Loss, and Ethics

William J. Kimberling1 , Ann F. Lindenmuth2
  • 1Director of the Center for the Study and Treatment of Usher Syndrome, Boys Town National Research Hospital, Professor of Biomedical Sciences, Creighton Medical School, Omaha, Nebraska
  • 2Graduate Student, School of Communication, University of Nebraska at Omaha, Omaha, Nebraska
Further Information

Publication History

Publication Date:
19 July 2007 (online)

Preview

ABSTRACT

In this article, some of the ethical issues arising from the applications derived from the genome project are addressed in relation to hearing loss and the deaf community. The authors present the issues as a series of questions that audiologists might pose to themselves and discuss with friends informally. Society has the obligation to find answers to these ethical questions. Audiologists, geneticists, and otolaryngologists have a unique understanding of hearing loss disorders and can act as advisors to the public and government officials. An understanding of the issues involved will help in generating a meaningful dialogue about the balance of individual rights with the needs of society.

REFERENCES

William J KimberlingPh.D. 

Director of the Center for the Study and Treatment of Usher Syndrome, Boys Town National Research Hospital

Creighton Medical School, Omaha, NE 68131

Email: kimber@boystown.org