Literature DB >> 12704639

Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease.

Cynthia A James1, Neil A Holtzman, Donald W Hadley.   

Abstract

Although recent research has investigated the attitudes of parents, professionals, and adult siblings toward carrier testing of minors, no studies have focused on the experiences of minor siblings of individuals with X-linked and autosomal recessive conditions. To explore adolescent sisters' perceptions of their reproductive risks, attitudes toward carrier testing, and resources for information and support, we interviewed 14 parents and 9 sisters (ages 12-15) of males with chronic granulomatous disease (CGD), a primary immunodeficiency disorder inherited in both an X-linked recessive and autosomal recessive fashion. Our semistructured telephone interviews were audiotaped, transcribed, and subjected to template analysis (a common qualitative methodology). Girls were all aware that CGD is an inherited condition and each had made an assessment of her reproductive risk. All girls considered their parents to be their best source of information and support, but girls had trouble initiating discussions for fear of upsetting their parents. All girls and parents considered eventual carrier testing vital for reproductive decision-making and relationship-building. However, girls favored carrier testing at a later age and expressed more concerns about psychological risks associated with testing than did their parents. When faced with the hypothetical situation of being offered carrier testing "tomorrow," half of the parents and untested daughters disagreed on the desirability of the test, with parents more likely to favor testing. Including adolescent sisters in family-based genetic counseling that provides an opportunity for age-appropriate discussion of inheritance and the timing, risks, and benefits of carrier testing would be beneficial to them. Published 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12704639     DOI: 10.1002/ajmg.c.10007

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  13 in total

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2.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

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4.  Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family.

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5.  Segmenting by risk perceptions: predicting young adults' genetic-belief profiles with health and opinion-leader covariates.

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7.  Parents' communication with siblings of children affected by an inherited genetic condition.

Authors:  Gillian Plumridge; Alison Metcalfe; Jane Coad; Paramjit Gill
Journal:  J Genet Couns       Date:  2011-04-19       Impact factor: 2.537

8.  Cool, but is it credible? Adolescents' and parents' approaches to genetic testing.

Authors:  Lynn Rew; Michael Mackert; Dan Bonevac
Journal:  West J Nurs Res       Date:  2010-08       Impact factor: 1.967

9.  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

10.  When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.

Authors:  Ramsey M Wehbe; Gail A Spiridigliozzi; Elizabeth M Heise; Deborah V Dawson; Allyn McConkie-Rosell
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

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