Literature DB >> 17952575

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

Christina G S Palmer1, Ariadna Martinez, Michelle Fox, Yvonne Sininger, Wayne W Grody, Lisa A Schimmenti.   

Abstract

As genetic testing becomes an integral part of the evaluation of deaf infants and children, it is important to understand parental views on genetic testing. The purpose of this study is to examine parental reasons for, and beliefs about, genetic testing for deafness in early-identified infants, and to determine if they differ as a function of ethnicity. We present baseline data collected from 56 Caucasian, 59 Hispanic, and 24 Asian parents of deaf children participating in a longitudinal, prospective study on genetic testing for connexin-related deafness. The overall finding is that reasons for, and beliefs about, genetic testing for deafness varied as a function of ethnicity. Virtually all parents sought genetic testing to understand why their child is deaf. However, Asian and/or Hispanic parents were more likely than Caucasian parents to view family planning, helping with their child's medical care, and helping the family as other important reasons for testing, and were more likely than Caucasian parents to perceive genetic testing to be useful for these purposes. Asian and Hispanic parents were more likely than Caucasian parents to perceive genetic testing in harmful terms. Genetic testing fulfills a cognitive need for parents to understand why their child is deaf, yet differences in responses suggest that Asian and Hispanic parents may seek testing for other purposes. Understanding different perspectives on genetic testing for deafness will enhance genetic counselors' cultural competence and facilitate the pre-test genetic counseling session.

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Year:  2007        PMID: 17952575     DOI: 10.1007/s10897-007-9134-z

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  37 in total

1.  Genetic testing for hearing loss: different motivations for the same outcome.

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2.  Genetic testing as part of the early hearing detection and intervention (EHDI) process.

Authors:  Lisa A Schimmenti; Ariadna Martinez; Michelle Fox; Barbara Crandall; Nina Shapiro; Milhan Telatar; Yvonne Sininger; Wayne W Grody; Christina G S Palmer
Journal:  Genet Med       Date:  2004 Nov-Dec       Impact factor: 8.822

3.  A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews.

Authors:  I Lerer; M Sagi; Z Ben-Neriah; T Wang; H Levi; D Abeliovich
Journal:  Hum Mutat       Date:  2001-11       Impact factor: 4.878

4.  A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

Authors:  Ignacio del Castillo; Manuela Villamar; Miguel A Moreno-Pelayo; Francisco J del Castillo; Araceli Alvarez; Dolores Tellería; Ibis Menéndez; Felipe Moreno
Journal:  N Engl J Med       Date:  2002-01-24       Impact factor: 91.245

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Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

6.  Controlled trial of pretest education approaches to enhance informed decision-making for BRCA1 gene testing.

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Journal:  J Natl Cancer Inst       Date:  1997-01-15       Impact factor: 13.506

7.  Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

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Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

8.  Language of early- and later-identified children with hearing loss.

Authors:  C Yoshinaga-Itano; A L Sedey; D K Coulter; A L Mehl
Journal:  Pediatrics       Date:  1998-11       Impact factor: 7.124

9.  A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness.

Authors:  Sarah K Burton; Kara Withrow; Kathleen S Arnos; Andrea L Kalfoglou; Arti Pandya
Journal:  Genet Med       Date:  2006-12       Impact factor: 8.822

Review 10.  GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review.

Authors:  Aileen Kenneson; Kim Van Naarden Braun; Coleen Boyle
Journal:  Genet Med       Date:  2002 Jul-Aug       Impact factor: 8.822

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  9 in total

1.  Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study.

Authors:  Patrick Boudreault; Erin E Baldwin; Michelle Fox; Loriel Dutton; Leeelle Tullis; Joyce Linden; Yoko Kobayashi; Jin Zhou; Janet S Sinsheimer; Yvonne Sininger; Wayne W Grody; Christina G S Palmer
Journal:  J Deaf Stud Deaf Educ       Date:  2010-05-20

2.  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

3.  Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry.

Authors:  Charles R Jonassaint; Eunice R Santos; Crystal M Glover; Perry W Payne; Grace-Ann Fasaye; Nefertiti Oji-Njideka; Stanley Hooker; Wenndy Hernandez; Morris W Foster; Rick A Kittles; Charmaine D Royal
Journal:  Hum Genet       Date:  2010-06-13       Impact factor: 4.132

4.  Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study.

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Journal:  Hum Genet       Date:  2012-10-30       Impact factor: 4.132

5.  "My Plate is Full": Reasons for Declining a Genetic Evaluation of Hearing Loss.

Authors:  Marci M Lesperance; Erin Winkler; Tori L Melendez; Beverly M Yashar
Journal:  J Genet Couns       Date:  2017-10-04       Impact factor: 2.537

6.  Genetic counseling and testing for Asian Americans: a systematic review.

Authors:  Jennifer L Young; Julie Mak; Talia Stanley; Michelle Bass; Mildred K Cho; Holly K Tabor
Journal:  Genet Med       Date:  2021-05-10       Impact factor: 8.822

7.  Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass.

Authors:  Lu Sun; Li-Jun Tan; Shu-Feng Lei; Xiang-Ding Chen; Xi Li; Rong Pan; Fang Yin; Quan-Wei Liu; Xiao-Feng Yan; Christopher J Papasian; Hong-Wen Deng
Journal:  PLoS One       Date:  2011-11-07       Impact factor: 3.240

8.  Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.

Authors:  Christina G S Palmer; Jason T Lueddeke; Jin Zhou
Journal:  Genet Med       Date:  2009-04       Impact factor: 8.822

9.  Parental attitudes to genetic testing differ by ethnicity and immigration in childhood nephrotic syndrome: a cross-sectional study.

Authors:  Karlota Borges; Jovanka Vasilevska-Ristovska; Neesha Hussain-Shamsy; Viral Patel; Tonny Banh; Diane Hebert; Rachel J Pearl; Seetha Radhakrishnan; Tino D Piscione; Christoph P B Licht; Valerie Langlois; Leo Levin; Lisa Strug; Rulan S Parekh
Journal:  Can J Kidney Health Dis       Date:  2016-03-17
  9 in total

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