Literature DB >> 10861663

Carrier testing in fragile X syndrome: effect on self-concept.

A McConkie-Rosell1, G A Spiridigliozzi, J A Sullivan, D V Dawson, A M Lachiewicz.   

Abstract

The purpose of the study was to explore self-concept in women at risk for inheriting the fragile X mutation. Time 1 measures were obtained prior to carrier testing and Time 2 measures were collected approximately 5 months after learning carrier status. The sample consisted of 42 women from 17 families. Measures included the Tennessee Self-Concept Scale (TSCS), the fragile X Visual Analog Scale (VAS), and a structured interview. The TSCS provided a global measure of self-concept and the fragile X VAS and structured interview provided a contextual measure of self related to carrier status. Results indicated that there were no differences initially between carriers and noncarriers and no change from Time 1 to Time 2 on the TSCS. Analysis of the Time 1 fragile X VAS means for the total sample found a reduction in positive feelings about self. Analysis of the Time 2 fragile X VAS found that noncarriers reported improvement in feelings about self, with no change in feelings about self found in the carriers. Responses from the structured interview indicated that the feelings regarding self in the context of genetic testing are not related to global self-concept, but result from concerns regarding the implications of a positive carrier test for themselves and their families. This information highlights areas related to carrier testing that warrant further investigation and may ultimately result in modifications to the genetic counseling. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10861663     DOI: 10.1002/1096-8628(20000619)92:5<336::aid-ajmg8>3.0.co;2-l

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  16 in total

Review 1.  Illness representations, self-regulation, and genetic counseling: a theoretical review.

Authors:  Shoshana Shiloh
Journal:  J Genet Couns       Date:  2006-10       Impact factor: 2.537

2.  Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.

Authors:  Allyn McConkie-Rosell; Jacqueline Del Giorno; Elizabeth Melvin Heise
Journal:  J Genet Couns       Date:  2010-09-28       Impact factor: 2.537

Review 3.  Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?

Authors:  Celine Lewis; Heather Skirton; Ray Jones
Journal:  J Genet Couns       Date:  2010-09-29       Impact factor: 2.537

4.  Living with genetic risk: effect on adolescent self-concept.

Authors:  Allyn McConkie-Rosell; Gail A Spiridigliozzi; Elizabeth Melvin; Deborah V Dawson; Ave M Lachiewicz
Journal:  Am J Med Genet C Semin Med Genet       Date:  2008-02-15       Impact factor: 3.908

5.  Guidelines for genetic testing of healthy children.

Authors: 
Journal:  Paediatr Child Health       Date:  2003-01       Impact factor: 2.253

6.  Extended family impact of genetic testing: the experiences of X-linked carrier grandmothers.

Authors:  Anna Lehmann; Beverley S Speight; Lauren Kerzin-Storrar
Journal:  J Genet Couns       Date:  2011-04-14       Impact factor: 2.537

7.  Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.

Authors:  Allyn McConkie-Rosell; Brenda Finucane; Amy Cronister; Liane Abrams; Robin L Bennett; Barbara J Pettersen
Journal:  J Genet Couns       Date:  2005-08       Impact factor: 2.537

8.  Women's attitudes toward testing for fragile X carrier status: a qualitative analysis.

Authors:  Aimee Anido; Lisa M Carlson; Lisa Taft; Stephanie L Sherman
Journal:  J Genet Couns       Date:  2005-08       Impact factor: 2.537

9.  Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome.

Authors:  Allyn McConkie-Rosell; Elizabeth Melvin Heise; Gail A Spiridigliozzi
Journal:  J Genet Couns       Date:  2009-03-11       Impact factor: 2.537

10.  Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders.

Authors:  Allyn McConkie-Rosell; Liane Abrams; Brenda Finucane; Amy Cronister; Louise W Gane; Sarah M Coffey; Stephanie Sherman; Lawrence M Nelson; Elizabeth Berry-Kravis; David Hessl; Sufen Chiu; Natalie Street; Ajay Vatave; Randi J Hagerman
Journal:  J Genet Couns       Date:  2007-05-12       Impact factor: 2.537

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