Literature DB >> 6454786

Objective knowledge about Huntington's disease and attitudes towards predictive tests of persons at risk.

B Teltscher, S Polgar.   

Abstract

The task of genetic counselling of people at risk for Huntington's disease might be facilitated by increased knowledge of relevant population characteristics. The aim of the present study was to clarify select socioeconomic characteristics, knowledge concerning the disease, and attitudes towards predictive tests of people at 50% risk of inheriting Huntington's disease in the state of Victoria. A random sample of subjects was drawn from the Huntington's disease register and 50 questionnaires were analysed. Respondents completed three questionnaires which covered their socioeconomic characteristics, the extent and accuracy of their knowledge about the genetic, progress, and treatment of Huntington's disease, and their attitude and acceptance of predictive tests as well as their intentions about future reproduction. A very positive attitude was found to be held by the respondents towards a predictive test if it was safe, reliable, and non-invasive. Resultant problems which would arise, should a reliable test be found, are discussed. The respondent's knowledge concerning the disease was found to be adequate generally.

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Year:  1981        PMID: 6454786      PMCID: PMC1048654          DOI: 10.1136/jmg.18.1.31

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  3 in total

1.  Attitudes of families to some aspects of Huntington's chorea.

Authors:  J Barette; C D Marsden
Journal:  Psychol Med       Date:  1979-05       Impact factor: 7.723

2.  Huntington's disease: the establishment of a national register.

Authors:  E Chiu; B Teltscher
Journal:  Med J Aust       Date:  1978-10-07       Impact factor: 7.738

3.  Attitudes of patients and their relatives to Huntington's disease.

Authors:  R Stern; R Eldridge
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

  3 in total
  8 in total

1.  Genetic testing preferences in families containing multiple individuals with epilepsy.

Authors:  Janice O Okeke; Virginia E Tangel; Shawn T Sorge; Dale C Hesdorffer; Melodie R Winawer; Jeff Goldsmith; Jo C Phelan; Wendy K Chung; Sara Shostak; Ruth Ottman
Journal:  Epilepsia       Date:  2014-09-29       Impact factor: 5.864

2.  Ethical dilemmas in clinical genetics.

Authors:  I D Young
Journal:  J Med Ethics       Date:  1984-06       Impact factor: 2.903

3.  Paradox of a better test for Huntington's disease.

Authors:  A Maat-Kievit; M Vegter-van der Vlis; M Zoeteweij; M Losekoot; A van Haeringen; R Roos
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-11       Impact factor: 10.154

4.  Some ethical issues in dementia research.

Authors:  B Mahendra
Journal:  J Med Ethics       Date:  1984-03       Impact factor: 2.903

Review 5.  Huntington's disease and the ethics of genetic prediction.

Authors:  G Terrenoire
Journal:  J Med Ethics       Date:  1992-06       Impact factor: 2.903

6.  Attitudes towards predictive testing in Huntington's disease: a recent survey in Belgium.

Authors:  G Evers-Kiebooms; J J Cassiman; H van den Berghe
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

7.  Attitudes of subjects at risk and their relatives towards genetic counselling in Huntington's chorea.

Authors:  A Tyler; P S Harper
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

8.  Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease.

Authors:  Elizabeth Penziner; Janet K Williams; Cheryl Erwin; Yvonne Bombard; Anne Wallis; Leigh J Beglinger; Michael R Hayden; Jane S Paulsen
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-04-05       Impact factor: 3.568

  8 in total

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