Genetic Testing and Genetic Counseling for Deafness: The Future Is Here
作者： Jeannie Weir Brunger , Anne L Matthews , Richard HJ Smith , Nathaniel H Robin , None
DOI: 10.1097/00005537-200104000-00027
关键词:
摘要: Today, genetic testing is an option for individuals who have deafness and hard-of-hearing conditions (D/HOH) their families diagnosis carrier detection. As more D/HOH genes are identified, will become commonplace. However, different from other tests that physicians commonly order therefore should be conducted differently. The objective of this study was to determine the best manner in which conduct D/HOH. Numerous studies shown pretest post-test counseling beneficial patients undergoing a variety conditions. need emphasized by our recently completed we found majority whose children had poor understanding many issues concerning recurrence risks meaning test results. We think integral part D/HOH.
sci-hub.se 参考文章(12)
M Hietala, A R Aro, A Hakonen, P Aula, P Niemelä, L Peltonen, Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland. American Journal of Human Genetics. ,vol. 56, pp. 1493- 1500 ,(1995)
Anna Middleton, J. Hewison, R.F. Mueller, Attitudes of deaf adults toward genetic testing for hereditary deafness. American Journal of Human Genetics. ,vol. 63, pp. 1175- 1180 ,(1998) , 10.1086/302060
Thomas Valère, The DNA vaccine website. http://www.genweb.com/Dnavax/ The Journal of Gene Medicine. ,vol. 1, pp. 295- 296 ,(1999) , 10.1002/(SICI)1521-2254(199907/08)1:4<295::AID-JGM52>3.0.CO;2-L
Alison Chapple, Carl May, Peter Campion, Lay understanding of genetic disease: A British study of families attending a genetic counseling service Journal of Genetic Counseling. ,vol. 4, pp. 281- 300 ,(1995) , 10.1007/BF01408074
E. S. Cohn, P. M. Kelley, T. W. Fowler, M. P. Gorga, D. M. Lefkowitz, H. J. Kuehn, G. B. Schaefer, L. S. Gobar, F. J. Hahn, D. J. Harris, W. J. Kimberling, Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1) Pediatrics. ,vol. 103, pp. 546- 550 ,(1999) , 10.1542/PEDS.103.3.546
Heidi L Rehm, Cynthia C Morton, A new age in the genetics of deafness. Genetics in Medicine. ,vol. 1, pp. 295- 304 ,(1999) , 10.1097/00125817-199909000-00009
KATHLEEN SHAVER ARNOS, JAMIE ISRAEL, MARGARET CUNNINGHAM, Genetic Counseling of the Deaf Annals of the New York Academy of Sciences. ,vol. 630, pp. 212- 222 ,(1991) , 10.1111/J.1749-6632.1991.TB19590.X
Jeanne Weir Brunger, Gail S Murray, Maryann O’Riordan, Anne L Matthews, Richard JH Smith, Nathaniel H Robin, None, Parental Attitudes toward Genetic Testing for Pediatric Deafness The American Journal of Human Genetics. ,vol. 67, pp. 1621- 1625 ,(2000) , 10.1086/316901
R H Kenen, R M Schmidt, Stigmatization of carrier status: social implications of heterozygote genetic screening programs. American Journal of Public Health. ,vol. 68, pp. 1116- 1120 ,(1978) , 10.2105/AJPH.68.11.1116
Moira Mennie, Mary Compton, Annette Gilfillan, R. A. Axton, W. A. Liston, I. Pullen, Dorothy Whyte, D. J. H. Brock, Prenatal screening for cystic fibrosis: attitudes and responses of participants Clinical Genetics. ,vol. 44, pp. 102- 106 ,(2008) , 10.1111/J.1399-0004.1993.TB03856.X