Literature DB >> 3976717

Transmitting balanced translocation carrier information within families: a follow-up study.

L Suslak, D M Price, F Desposito.   

Abstract

Approximately 1 of 500 individuals is a carrier of a balanced chromosome translocation. Since many translocations are inherited, many (but not all) relatives of carriers have a need to be informed of their potential carrier status. Presently, no data are available as to what extent individuals identified as balanced carriers inform at-risk relatives of the problem. We interviewed 12 balanced translocation carriers to learn whether such information had been transmitted to relatives. The 12 propositi had 36 surviving sibs and 21 surviving parents. Of the 36 sibs, 32 were informed of their risk. The four sibs not informed were from two families. Only 16 of the 32 informed sibs had subsequent carrier testing. Of the 21 surviving parents, 14 were told by their children of their carrier status; subsequently, three parent couples were tested. This survey provides data showing that individuals do not always disclose genetic risk information to relatives. Therefore, genetic professionals need to determine if they have a duty to transmit such information to at-risk relatives in light of the harm that may occur when information is withheld.

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Year:  1985        PMID: 3976717     DOI: 10.1002/ajmg.1320200204

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


  8 in total

1.  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

2.  Family Communication and Genetic Counseling: The Case of Hereditary Breast and Ovarian Cancer.

Authors:  J Green; M Richards; F Murton; H Statham; N Hallowell
Journal:  J Genet Couns       Date:  1997-03       Impact factor: 2.537

3.  DNA testing for fragile X syndrome: implications for parents and family.

Authors:  M A van Rijn; B B de Vries; A Tibben; A M van den Ouweland; D J Halley; M F Niermeijer
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

4.  A family genetic risk communication framework: guiding tool development in genetics health services.

Authors:  Miriam E Wiens; Brenda J Wilson; Christina Honeywell; Holly Etchegary
Journal:  J Community Genet       Date:  2013-01-15

5.  Two siblings with unbalanced t(10;21) translocations and non-neuropathic neuropathic bladder.

Authors:  Mandela Thyoka; Alex Henderson; Bozena Starzyk; Anupam Lall
Journal:  BMJ Case Rep       Date:  2014-02-07

6.  Improving service evaluation in clinical genetics: identifying effects of genetic diseases on individuals and families.

Authors:  Marion McAllister; Katherine Payne; Stuart Nicholls; Rhona MacLeod; Dian Donnai; Linda M Davies
Journal:  J Genet Couns       Date:  2007-02-13       Impact factor: 2.537

7.  Informing children of their newborn screening carrier result for sickle cell or cystic fibrosis: qualitative study of parents' intentions, views and support needs.

Authors:  Fiona Ulph; Tim Cullinan; Nadeem Qureshi; Joe Kai
Journal:  J Genet Couns       Date:  2013-12-04       Impact factor: 2.537

8.  Attitudes of physicians and patients towards disclosure of genetic information to spouse and first-degree relatives: a case study from Turkey.

Authors:  Aslihan Akpinar; Nermin Ersoy
Journal:  BMC Med Ethics       Date:  2014-05-16       Impact factor: 2.652

  8 in total

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