Literature DB >> 9187678

Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations.

K Madan1, A W Nieuwint, Y van Bever.   

Abstract

We report an unusual case of a balanced reciprocal translocation with a recombinant chromosome which has arisen from a familial balanced complex translocation. Fluorescence in situ hybridization studies were essential for the identification of the breakpoints. A review of 60 cases of balanced complex translocations (BCT) has revealed three cases similar to ours. Carriers of BCT have a high risk of having spontaneous abortions or a child with an unbalanced karyotype. Certain types of balanced rearrangements involving an insertion can give rise to a simpler balanced translocation as a result of crossover. Our observations support the assumption that the chance that a de novo balanced complex translocation is associated with an abnormal phenotype increases with the number of breakpoints.

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Year:  1997        PMID: 9187678     DOI: 10.1007/s004390050453

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  33 in total

1.  Delineation of complex chromosomal rearrangements: evidence for increased complexity.

Authors:  Caroline Astbury; Laurie A Christ; David J Aughton; Suzanne B Cassidy; Atsuko Fujimoto; Beth A Pletcher; Irwin A Schafer; Stuart Schwartz
Journal:  Hum Genet       Date:  2004-02-07       Impact factor: 4.132

2.  Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD.

Authors:  Paul N Scriven; Susan M Bint; Angela F Davies; Caroline Mackie Ogilvie
Journal:  Eur J Hum Genet       Date:  2013-10-16       Impact factor: 4.246

Review 3.  Complex human chromosomal and genomic rearrangements.

Authors:  Feng Zhang; Claudia M B Carvalho; James R Lupski
Journal:  Trends Genet       Date:  2009-06-25       Impact factor: 11.639

4.  Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.

Authors:  Julia Baptista; Catherine Mercer; Elena Prigmore; Susan M Gribble; Nigel P Carter; Viv Maloney; N Simon Thomas; Patricia A Jacobs; John A Crolla
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

5.  A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.

Authors:  Natalia Trpchevska; Ivanka Dimova; Tatyana Arabadji; Tanya Milachich; Svetlana Angelova; Magdalena Dimitrova; Mariela Hristova-Savova; Petya Andreeva; Tania Timeva; Atanas Shterev
Journal:  J Assist Reprod Genet       Date:  2017-02-24       Impact factor: 3.412

6.  Familial complex chromosome rearrangement (CCR) involving 5 breakpoints on chromosomes 1, 3 and 13 in a severe oligozoospermic patient.

Authors:  Lin Li; Xueyuan Heng; Wang Yun; Shuqi Zheng; Jixia Zhang; Wufang Fan
Journal:  J Assist Reprod Genet       Date:  2013-02-05       Impact factor: 3.412

7.  A novel male 2;4;14 complex chromosomal translocation with normal semen parameters but 100% embryonic aneuploidy.

Authors:  Jade Mas; Reem Sabouni; Silvina Bocca
Journal:  J Assist Reprod Genet       Date:  2018-01-29       Impact factor: 3.412

8.  Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics history.

Authors:  Pritti K Priya; Vineet V Mishra; Thomas Liehr; Monika Ziegler; Stuti Tiwari; Alpesh Patel; Shiva Shankar Chettiar; Hetvi Patel
Journal:  J Assist Reprod Genet       Date:  2018-01-23       Impact factor: 3.412

9.  Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report.

Authors:  Paula Jp de Vree; Marleen Eh Simon; Marieke F van Dooren; Gerda Ht Stoevelaar; José Tw Hilkmann; Michel A Rongen; Gido Cm Huijbregts; Annemieke Jmh Verkerk; Pino J Poddighe
Journal:  Mol Cytogenet       Date:  2009-07-13       Impact factor: 2.009

Review 10.  Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.

Authors:  Martin Poot; Thomas Haaf
Journal:  Mol Syndromol       Date:  2015-08-15
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