Literature DB >> 152585

Stigmatization of carrier status: social implications of heterozygote genetic screening programs.

R H Kenen, R M Schmidt.   

Abstract

Possible latent psychological and social consequences ensuing from genetic screening programs need to be investigated during the planning phase of national genetic screening programs. The relatively few studies which have been performed to determine psychological, social, and economic consequences resulting from a genetic screening program are reviewed. Stigmatization of carrier-status, having major psychosocial implications in heterozygote genetic screening programs, is discussed and related to Erving Goffman's work in the area of stigmatization. Questions are raised regarding the relationship between such variables as religiosity and sex of the individual and acceptance of the status of newly identified carrier of a mutant gene. Severity of the deleterious gene and visibility of the carrier status are two important factors to consider in an estimation of potential stigma. Specific implications are discussed for four genetic diseases: Tay-Sachs, Sickle-Cell Anemia, Huntington's disease and Hemophilia.

Entities:  

Keywords:  Genetics and Reproduction

Mesh:

Year:  1978        PMID: 152585      PMCID: PMC1654013          DOI: 10.2105/ajph.68.11.1116

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  14 in total

1.  Tay-Sachs screening: social and psychological impact.

Authors:  B Childs; L Gordis; M M Kaback; H H Kazazian
Journal:  Am J Hum Genet       Date:  1976-11       Impact factor: 11.025

2.  The religous factor and the role of gulit in parental acceptance of the retarded child.

Authors:  G H ZUK
Journal:  Am J Ment Defic       Date:  1959-07

3.  On cooling the mark out; some aspects of adaptation to failure.

Authors:  E GOFFMAN
Journal:  Psychiatry       Date:  1952-11       Impact factor: 2.458

4.  Alternative models of counseling for genetic disorders.

Authors:  V E Headings
Journal:  Soc Biol       Date:  1975

5.  Genetic clinic. A follow-up.

Authors:  C O Carter; J A Roberts; K A Evans; A R Buck
Journal:  Lancet       Date:  1971-02-06       Impact factor: 79.321

6.  Genetic counseling: a consumers' view.

Authors:  C O Leonard; G A Chase; B Childs
Journal:  N Engl J Med       Date:  1972-08-31       Impact factor: 91.245

7.  Some negative aspects of state health departments' policies related to screening for sickle cell anemia.

Authors:  I M Rutkow; J M Lipton
Journal:  Am J Public Health       Date:  1974-03       Impact factor: 9.308

8.  Psychosocial effects of sickle cell disease.

Authors:  C F Whitten; J Fischhoff
Journal:  Arch Intern Med       Date:  1974-04

9.  Awareness of sickle cell abnormalities. A medical and lay community problem.

Authors:  W I Young; J Peters; H B Houser; E B Jackson
Journal:  Ohio State Med J       Date:  1974-01

10.  A comparison of the physical and intellectual development of black children with and without sickle-cell trait.

Authors:  M K McCormack; S Scarr-Salapatek; H Polesky; W Thompson; S H Katz; W B Barker
Journal:  Pediatrics       Date:  1975-12       Impact factor: 7.124

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  16 in total

Review 1.  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

2.  Threat to Parental Role: A Possible Mechanism of Altered Self-Concept Related to Carrier Knowledge.

Authors:  A McConkie-Rosell; B M DeVellis
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

3.  A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.

Authors:  E W Almqvist; M Bloch; R Brinkman; D Craufurd; M R Hayden
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

Review 4.  Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.

Authors:  Jeffrey R Botkin; John W Belmont; Jonathan S Berg; Benjamin E Berkman; Yvonne Bombard; Ingrid A Holm; Howard P Levy; Kelly E Ormond; Howard M Saal; Nancy B Spinner; Benjamin S Wilfond; Joseph D McInerney
Journal:  Am J Hum Genet       Date:  2015-07-02       Impact factor: 11.025

5.  Involvement of rabbis in counseling and referral for genetic conditions: results of a survey.

Authors:  P Steiner-Grossman; K L David
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

6.  The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

7.  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

8.  Sickle cell trait counseling-evaluation of counselors and counselees.

Authors:  C F Whitten; J F Thomas; E N Nishiura
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025

9.  Parental attitudes toward genetic testing for pediatric deafness.

Authors:  J W Brunger; G S Murray; M O'Riordan; A L Matthews; R J Smith; N H Robin
Journal:  Am J Hum Genet       Date:  2000-11-02       Impact factor: 11.025

10.  Perception, experience, and response to genetic discrimination in Huntington's disease: the Australian results of The International RESPOND-HD study.

Authors:  Anita M Y Goh; Edmond Chiu; Olga Yastrubetskaya; Cheryl Erwin; Janet K Williams; Andrew R Juhl; Jane S Paulsen
Journal:  Genet Test Mol Biomarkers       Date:  2013-01-04
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