Literature DB >> 20302980

Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management.

Sandrine Leclercq1, Jacques Auger, Céline Dupont, Dominique Le Tessier, Aziza Lebbar, Françoise Baverel, Jean Michel Dupont, Florence Eustache.   

Abstract

Numerous studies have shown that balanced reciprocal or Robertsonian translocations and inversions are associated with reduced or absent sperm production. In contrast, a similar association has been rarely reported for unbalanced translocations. An unbalanced translocation, 45,XY,-15,der(18)t(15;18)(q11.2;q23), was found in two healthy infertile brothers who were referred to our hospital together with their partners for infertility. At least two routine semen analyses and karyotyping were done for each of the brothers. Sperm meiotic segregation was studied for both with a three-color FISH assay using locus-specific probes. Semen analyses showed a severe oligo-astheno-teratozoospermia with remarkably similar profiles in the two brothers. The unbalanced translocation had a deletion of 15pter-15q11.2 as well as a deletion of 18q23-18qter. The meiotic segregation was similar in the two brothers with a prevalence of alternate segregation mode. However, no phenotypic effect in the offspring can be expected only if the normal chromosomes 15 and 18 are transmitted to progeny. According to the sperm FISH results, the theoretical probability of this happening is about 25%. Based on the overall results, genetic and reproductive counselling was offered to both couples. Finally, both couples chose the alternative of donor insemination rather than preimplantation genetic diagnosis. The present study helps delineating a phenotypically silent CNV at the distal part of chromosome 18 long arm and illustrates the advantages of an integrated multidisciplinary genetic, reproductive and psychological approach to give the best possible assistance to couples who are faced with a complex and distressing genetic cause of infertility. Copyright 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20302980     DOI: 10.1016/j.ejmg.2010.03.003

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  4 in total

1.  Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby.

Authors:  De-Hua Cheng; Fei Gong; Chang-Fu Lu; Lu-Yun Li; Guang-Xiu Lu; Yue-Qiu Tan
Journal:  J Assist Reprod Genet       Date:  2012-09-22       Impact factor: 3.412

2.  Impact of reciprocal translocation t (18; 21) on male infertility and embryo development: lessons from an oocyte-donating ICSI cycle.

Authors:  Longjie Gu; Hanwang Zhang; Guijin Zhu
Journal:  J Assist Reprod Genet       Date:  2011-04-01       Impact factor: 3.412

3.  Novel Y chromosome breakpoint in an infertile male with a de novo translocation t(Y;16): a case report.

Authors:  Yu-Ting Jiang; Hong-Guo Zhang; Rui-Xue Wang; Yang Yu; Zhi-Hong Zhang; Rui-Zhi Liu
Journal:  J Assist Reprod Genet       Date:  2012-11-15       Impact factor: 3.412

4.  Characterization by microarray and meiotic segregation study of a der(10)t(10;18) in a patient with infertility and normal phenotype.

Authors:  Stephan Kemeny; Florence Brugnon; Eléonore Eymard-Pierre; Carole Goumy; Laurent Janny; Andreï Tchirkov; Christine Francannet; Philippe Vago; Céline Pebrel-Richard
Journal:  Asian J Androl       Date:  2017 Jan-Feb       Impact factor: 3.285

  4 in total

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