Literature DB >> 2736789

Genetic counseling in families with inherited balanced translocations: experience with 36 families.

G Wolff1, E Back, S Arleth, U Rapp-Körner.   

Abstract

We report on genetic counseling and investigations in 36 families with inherited balanced translocations ascertained in different ways, with special regard to the completeness and reasons for incompleteness of family investigation. Quantitative evaluation of the results of cytogenetic investigations shows that non-directive genetic counseling was very effective in many families. Yet, in most of the families (34) genetic counseling and investigation remained incomplete in the sense that not all living potential translocation carriers could be counseled or investigated or that the origin of a fresh mutation could not be established by a normal karyotype in the parents of a carrier. Only in seven families could nearly all living potential carriers be counseled and investigated. The most frequent reason for incompleteness was the impossibility of transmitting or refusal to transmit information about the genetic risks to relatives (21 families), whereas direct rejection of investigation by a counseled individual was a rather rare event (18 adults). Families ascertained because of an unbalanced child seem to be more willing to transmit genetic information to relatives than families ascertained in other ways. Non-directive genetic counseling gave us an insight into the emotional problems arising during counseling of translocation families.

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Year:  1989        PMID: 2736789     DOI: 10.1111/j.1399-0004.1989.tb02965.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

Review 1.  Inappropriate genetic testing of children.

Authors:  A Fryer
Journal:  Arch Dis Child       Date:  2000-10       Impact factor: 3.791

2.  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

3.  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

4.  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

5.  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

6.  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

  6 in total

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