Genetics Content in the Graduate Audiology Curriculum

Author:

Arnos Kathleen S.12,Rocca Maria G. Della1,Karchmer Michael A.1,Culpepper Brandt3,Cohn Wendy F.4

Affiliation:

1. Gallaudet University, Washington, DC

2. Genetics Program, Department of Biology, Gallaudet University, 800 Florida Avenue, NE, Washington, DC 20002

3. Towson State University, Towson, MD

4. University of Virginia School of Medicine, Charlottesville

Abstract

Astounding progress has been made in the identification and characterization of genes for hearing loss, which has led to an increasing role of genetics evaluation and testing in the diagnostic process for children with hearing loss. The importance of health professionals such as audiologists gaining core competencies in genetics has been recognized. The current report describes a survey of academic programs in audiology designed to determine the extent to which genetics content is included in the curriculum. Responses from 56% of existing academic programs indicate that 95% include some genetics content in their programs, with the total number of classroom hours ranging from 2 to 65. Most programs included information on basic genetic mechanisms, syndromes, and interpreting family history information, while many fewer reported covering the molecular basis of hearing loss, genetic testing, or ethical or legal issues. The results of this survey demonstrate the need to incorporate more genetics content into audiology curricula and suggest strategies for assisting audiology faculty with this process.

Publisher

American Speech Language Hearing Association

Subject

Speech and Hearing

Reference29 articles.

1. The implications of genetic testing for deafness;Arnos K. S.;Ear & Hearing,2003

2. Association of Professors of Human or Medical Genetics. (n.d.) National Coalition for Health Professional Education in Genetics (NCHPEG) Guidelines. Retrieved January 8 2004 from http://www.faseb.org/genetics/aphmg/guidelines.htm

3. Parental attitudes toward genetic testing for pediatric deafness;Brunger J. W.;American Journal of Human Genetics,2000

4. Survey of speech-language pathologists’ and audiologists’ knowledge of clinical genetics;Chermak G. D.;ASHA,1993

5. Clinical studies of families with hearing loss attributable to mutations in the Connexin 26 gene (GJB2/DFNB1);Cohn E. S.;Pediatrics,1999

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