Literature DB >> 9030039

Benefits and burdens of genetic carrier identification.

J K Williams1, D L Schutte.   

Abstract

This qualitative study examined experiences of adults requesting genetic-carrier testing for four autosomal-recessive and X-linked-recessive disorders. The sample consisted of 34 adults with a positive family history or membership in an ethnic group at risk for the inherited disorder. A semistructured interview guide was used to collect data during an interview 1 month after receipt of test results. Noncarriers experienced benefits of emotional relief and freedom to move ahead with reproductive planning. Carriers experienced burdens of sadness and loss of reproductive expectations. Some subjects in both groups experienced difficulty disclosing results to selected family members and expressed concerns regarding disclosure of testing to insurance providers.

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Mesh:

Year:  1997        PMID: 9030039     DOI: 10.1177/019394599701900105

Source DB:  PubMed          Journal:  West J Nurs Res        ISSN: 0193-9459            Impact factor:   1.967


  13 in total

1.  Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation.

Authors:  O Järvinen; A M Aalto; A E Lehesjoki; M Lindlöf; I Söderling; A Uutela; H Kääriäinen
Journal:  J Med Genet       Date:  1999-08       Impact factor: 6.318

Review 2.  State of the science: social, psychological, and ethical nursing research in genetics.

Authors:  G Anderson
Journal:  Biol Res Nurs       Date:  1999-10       Impact factor: 2.522

3.  Implications of carrier identification in newborn screening for cystic fibrosis.

Authors:  E P Parsons; A J Clarke; D M Bradley
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2003-11       Impact factor: 5.747

Review 4.  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

5.  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

6.  Psychosocial Responses to being Identified as a Balanced Chromosomal Translocation Carrier: a Qualitative Investigation of Parents in Japan.

Authors:  Mikiko Kaneko; Hirofumi Ohashi; Tomoko Takamura; Hiroshi Kawame
Journal:  J Genet Couns       Date:  2015-03-20       Impact factor: 2.537

7.  Attitudes towards potentially carrying the FMR1 premutation: before vs after testing of non-carrier females with diminished ovarian reserve.

Authors:  Lisa M Pastore; Maria Antero; Karen Ventura; J Kim Penberthy; Semara A Thomas; Logan B Karns
Journal:  J Genet Couns       Date:  2014-05-03       Impact factor: 2.537

8.  Using the impact of event scale to evaluate psychological response to being a phenylketonuria gene carrier.

Authors:  Catherine Y Read
Journal:  J Genet Couns       Date:  2004-06       Impact factor: 2.537

9.  Emotional reaction to fragile X premutation carrier tests among infertile women.

Authors:  Lisa M Pastore; Wendy L Morris; Logan B Karns
Journal:  J Genet Couns       Date:  2007-10-30       Impact factor: 2.537

10.  Experiences of Being Heterozygous for Fabry Disease: a Qualitative Study.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2016-03-07       Impact factor: 2.537

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