Literature DB >> 2750783

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

A Daniel1, E B Hook, G Wulf.   

Abstract

Data on 1,237 prenatal (amniocyte) diagnoses in cases of familial chromosome rearrangements were collated from 79 American and Canadian laboratories. These were added to European data (Daniel et al: Prenatal Diagn 6:315-350, 1986) on 596 reciprocal translocations (rcp) from 71 collaborative laboratories. The total data set was examined for relationships between balanced or unbalanced result and mode of ascertainment, sex of carrier parent, chromosomes involved, and (in cases of reciprocal translocations and pericentric inversions) for potential or actual chromosome imbalance size (% haploid autosome length). Risk rates for unbalanced segregants were markedly dissimilar. These ranged from approximately 50% down to essentially a negligible risk. The risk was approximately 50% for carriers of the following: complex chromosome rearrangements (ccr); insertions (ins); and for 2:2 segregating rcp ascertained by mode 1 (term unbalanced proband) with small imbalance segments. Pooled carriers (either sex) of 2:2 segregating rcp of mode 1 had a risk of 20-25% whereas female Robertsonian (rob) translocation (D;21) carriers and pericentric inversion (pii) carriers of pii with small distal segments had a risk of 10-15%. Pooled 2:2 segregating rcp carriers ascertained by mode 2 (a couple with recurrent miscarriages) and male carriers of rob (D;21) had a risk of 1.5-5%. The risk of unbalanced segregants was 1-2% (in this data) for male and female rob (13;14) carriers and for pooled pericentric inversion carriers. However, for carriers of most "type" (recurrent breakpoints) pii, for all paracentric inversions, and (as expected) for rob not involving 13 or 21, there were no term unbalanced progeny. For 2:2 segregating reciprocal translocations plots were prepared that could be used to determine broad risk groups for carriers of such rcp. In 3:1 segregating rcp there were 3.3 times fewer male than female carriers, whereas there were 1.3 times fewer male carriers in 2:2 segregating rcp. In 2:2 segregating rcp there is little effect on the fertility of male carriers and risks of unbalanced progeny were found to be equal to those for female carriers, whereas in the 3:1 segregating rcp, risks were much less for male as compared to female carriers. This indicates that 3:1 segregating rep are more similar to Robertsonian translocations in their greater effect on the fertility of male carriers.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1989        PMID: 2750783     DOI: 10.1002/ajmg.1320330105

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


  26 in total

1.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

Review 2.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  Paracentric inversion of chromosome 15(q15q24): description of three families.

Authors:  E D'Alessandro; C De Matteis; M L Lo Re; M Di Cola; C Ligas; F Cappa; G Del Porto
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

4.  A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.

Authors:  Vaidehi Jobanputra; Wendy K Chung; April M Hacker; Beverly S Emanuel; Dorothy Warburton
Journal:  Prenat Diagn       Date:  2005-08       Impact factor: 3.050

5.  Paracentric inversion 11q in Canadian Hutterites.

Authors:  B N Chodirker; C R Greenberg; P D Pabello; A E Chudley
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

6.  Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.

Authors:  Alejandra Vázquez-Cárdenas; Ana I Vásquez-Velásquez; Patricio Barros-Núñez; Johana Mantilla-Capacho; Mariano Rocchi; Horacio Rivera
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

7.  Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).

Authors:  N Simon Thomas; Viv Maloney; Victoria Bryant; Shuwen Huang; Carole Brewer; Katherine Lachlan; Patricia A Jacobs
Journal:  Hum Genet       Date:  2008-12-24       Impact factor: 4.132

8.  Investigation of the origins of human autosomal inversions.

Authors:  N Simon Thomas; Victoria Bryant; Vivienne Maloney; Annette E Cockwell; Patricia A Jacobs
Journal:  Hum Genet       Date:  2008-05-10       Impact factor: 4.132

9.  First-trimester combined screening is effective for the detection of unbalanced chromosomal translocations at 11 to 12 weeks of gestation.

Authors:  Shangyu Huang; Chialin Chang; Pojen Cheng; Chinghua Hsiao; Yungkuei Soong; Tao Duan
Journal:  Reprod Sci       Date:  2013-10-31       Impact factor: 3.060

10.  At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors:  D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

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