Literature DB >> 11062052

Parental attitudes toward genetic testing for pediatric deafness.

J W Brunger1, G S Murray, M O'Riordan, A L Matthews, R J Smith, N H Robin.   

Abstract

Recent molecular genetic advances have resulted in genetic testing becoming an option for deaf individuals and their families. However, there is little information about the interest in such testing. To investigate this issue, parents with normal hearing who have one or more deaf children were surveyed about their attitudes toward diagnostic, carrier, and prenatal genetic testing for deafness. This population was chosen because it represents the majority of individuals who are encountered in clinical practice, given that 90%-95% of deaf individuals are born to persons with normal hearing. Of 328 surveys distributed, 96 were completed and returned. Of the respondents, 96% recorded a positive attitude toward genetic testing for deafness, including prenatal testing, although none would use this information to terminate an affected pregnancy. All respondents had a poor understanding of genetics, with 98% both incorrectly estimating the recurrence risk of deafness and misunderstanding the concept of inheritance. Notably, these findings were similar in the group who had had genetic testing for their children and in the group who had not, suggesting either that the parents who received genetic testing did not receive genetic counseling or that the counseling was not effective. On the basis of these results, it was concluded that this population is interested in the use of genetic testing and that testing should not be done without first providing formal genetic counseling. Appropriate counseling can help parents to understand the risks, benefits, and limitations of genetic testing.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2000        PMID: 11062052      PMCID: PMC1287942          DOI: 10.1086/316901

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  13 in total

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Review 2.  Recurrence risks.

Authors:  S D Smith
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

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Authors:  D Koehn; K Morgan; F C Fraser
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4.  Screening and genetic counseling for beta-thalassemia trait in a population unselected for interest: comparison of three counseling methods.

Authors:  P T Rowley; M Lipkin; L Fisher
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

5.  Community attitudes to cystic fibrosis carrier testing in England: a pilot study.

Authors:  R Williamson; M E Allison; T J Bentley; S M Lim; E Watson; J Chapple; S Adam; M Boulton
Journal:  Prenat Diagn       Date:  1989-10       Impact factor: 3.050

6.  Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

Authors:  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
Journal:  Pediatrics       Date:  1999-03       Impact factor: 7.124

7.  Prenatal screening for cystic fibrosis: attitudes and responses of participants.

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8.  Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.

Authors:  M Hietala; A Hakonen; A R Aro; P Niemelä; L Peltonen; P Aula
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

9.  Attitudes of deaf adults toward genetic testing for hereditary deafness.

Authors:  A Middleton; J Hewison; R F Mueller
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025

10.  Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

Authors:  L Zelante; P Gasparini; X Estivill; S Melchionda; L D'Agruma; N Govea; M Milá; M D Monica; J Lutfi; M Shohat; E Mansfield; K Delgrosso; E Rappaport; S Surrey; P Fortina
Journal:  Hum Mol Genet       Date:  1997-09       Impact factor: 6.150

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  33 in total

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2.  Consumers' desire towards current and prospective reproductive genetic testing.

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3.  Correlates of genetic counseling and testing among Orthodox Jews.

Authors:  Shulamis Juni Pollak
Journal:  J Relig Health       Date:  2009-08-11

4.  Genetic knowledge and attitudes of parents of children with congenital heart defects.

Authors:  Sara M Fitzgerald-Butt; Jennifer Klima; Kelly Kelleher; Deena Chisolm; Kim L McBride
Journal:  Am J Med Genet A       Date:  2014-09-24       Impact factor: 2.802

Review 5.  Ethical and social implications of genetic testing for communication disorders.

Authors:  Kathleen S Arnos
Journal:  J Commun Disord       Date:  2008-03-25       Impact factor: 2.288

6.  Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.

Authors:  Danya F Vears; Clare Delany; John Massie; Lynn Gillam
Journal:  J Genet Couns       Date:  2016-05-19       Impact factor: 2.537

7.  A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.

Authors:  Christina G S Palmer; Ariadna Martinez; Michelle Fox; Jin Zhou; Nina Shapiro; Yvonne Sininger; Wayne W Grody; Lisa A Schimmenti
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

8.  Ethnic differences in parental perceptions of genetic testing for deaf infants.

Authors:  Christina G S Palmer; Ariadna Martinez; Michelle Fox; Yvonne Sininger; Wayne W Grody; Lisa A Schimmenti
Journal:  J Genet Couns       Date:  2007-10-19       Impact factor: 2.537

9.  Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.

Authors:  Sara M Fitzgerald-Butt; Lindsey Byrne; Cynthia A Gerhardt; Kathryn Vannatta; Timothy M Hoffman; Kim L McBride
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10.  Examining the relationship between genetic counselors' attitudes toward deaf people and the genetic counseling session.

Authors:  Emily E Enns; Patrick Boudreault; Christina G S Palmer
Journal:  J Genet Couns       Date:  2009-11-11       Impact factor: 2.537

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