Journal of Reproduction & Infertility

Journal of Reproduction & Infertility

Inter-chromosomal Effect in a Robertsonian Translocation (13;14) Carrier with a Child Affected by Down Syndrome: A Case Report

Authors
1 Dr. F. Nabipour Pathobiology laboratory, Kerman, Iran
2 Department of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran
3 Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran
Abstract
Background: Although the balanced carriers of Robertsonian translocations (ROBs) typically exhibit normal phenotypes, they may experience recurrent abortions or have offspring with chromosomal disorders. A proposed mechanism is the inter-chromosomal effect (ICE), where disrupted meiotic segregation may increase aneuploid gamete production. This study presents a male case carrier of t(13;14) who had a deceased child with Down syndrome (DS) and investigates t(13;14) as a potential factor contributing to the birth of a child with DS. Case Presentation: A couple with a history of recurrent abortions and a deceased child with DS was referred to a medical genetics laboratory. Karyotype analysis revealed that the male partner was a carrier of t(13;14) (45,XY,t(13;14)), while the female partner had a normal karyotype. The couple’s subsequent pregnancy resulted in a healthy female fetus inheriting t(13;14). The deceased child had a karyotype of 47, XY, +21, consistent with DS. In this study, the role of t(13;14) and ICE as potential contributors to the birth of a child with DS was explored. Conclusion: Prenatal screening for carriers of ROBs is strongly recommended to assess the risk of unbalanced chromosomal disorders in offspring.
Keywords

  1. Li PK, Lai FM, Lee JC, Lai KN. Glomemlonephritis associated with robertsonian translocation t (13; 14). Nephron. 1992;62(2):220-3.
  2. Anton E, Blanco J, Egozcue J, Vidal F. Sperm FISH studies in seven male carriers of Robertsonian translocation t (13; 14)(q10; q10). Hum Reprod. 2004;19(6):1345-51.
  3. Malekpour N, Kormi SMA, Azadbakht M, Yousefi M, Hasanzadeh-Nazar Abadi M. The survey of double Robertsonian translocation 13q; 14q in the pedigree of 44; XX woman: a case report. Int J Mol Cell Med. 2017;6(4):243-8.
  4. Alfarawati S, Fragouli E, Colls P, Wells D. Embryos of robertsonian translocation carriers exhibit a mitotic interchromosomal effect that enhances genetic instability during early development. PLoS Genet. 2012;8(10):e1003025.
  5. Jaiswal S, Upadhyay A, Ali A, Upadhyay S, Kumar A, Rai A. Two familial cases of robertsonian translocations 13; 14 and its clinical consequences. J Genet Syndr Gene Ther. 2016;7(1):1-4.
  6. Sahraeean S, Jebelli A, Shahbazi Z, Piryaei F. Homozygosity for robertsonian translocation (14q; 15q) in a newborn with a familial history of recurrent abortion and newborns affected by hepatosplenomegaly: a case report. J Reprod Infertil. 2023;24(4):301-5.
  7. Allen EG, Freeman SB, Druschel C, Hobbs CA, O’Leary LA, Romitti PA, et al. Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects. Hum Genet. 2009;125(1):41-52.
  8. Lejeune J. Autosomal disorders. Pediatrics. 1963;32:326-37.
  9. Mateu-Brull E, Rodrigo L, Peinado V, Mercader A, Campos-Galindo I, Bronet F, et al. Interchromosomal effect in carriers of translocations and inversions assessed by preimplantation genetic testing for structural rearrangements (PGT-SR). J Assist Reprod Genet. 2019;36(12):2547-55.
  10. Rogenhofer N, Dürl S, Ochsenkühn R, Neusser M, Aichinger E, Thaler C, et al. Case report: elevated sperm aneuploidy levels in an infertile Robertsonian translocation t (21; 21) carrier with possible interchromosomal effect. J Assist Reprod Genet. 2012;29(4):343-6.
  11. Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, et al. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. Am J Hum Genet. 1996;58(3):628-33.
  12. Miryounesi M, Diantpour M, Motevaseli E, Ghafouri-Fard S. Homozygosity for a Robertsonian translocation (13q; 14q) in a phenotypically normal 44, xx female with a history of recurrent abortion and a normal pregnancy outcome. J Reprod Infertil. 2016;17(3):184-7.
  13. Xu S, Tang D, Fang K, Xia Y, Song J, Wang W, et al. Analysis of meiotic segregation patterns and interchromosomal effects in sperm from a Robertsonian translocation family. Biomed Res. 2014;25(2):233-9.
  14. Douet-Guilbert N, Bris MJ, Amice V, Marchetti C, Delobel B, Amice J, Braekeleer MD, Morel F. Interchromosomal effect in sperm of males with translocations: report of 6 cases and review of the literature. Int J Androl. 2005;28(6):372-9.
  15. Comazzetto S, Di Giacomo M, Rasmussen KD, Much C, Azzi C, Perlas E, et al. Oligoasthenoteratozoospermia and infertility in mice deficient for miR-34b/c and miR-449 loci. PLoS Genet. 2014;10(10):e1004597.
  16. Korenberg JR, Chen X, Schipper R, Sun Z, Gonsky R, Gerwehr S, et al. Down syndrome phenotypes: the consequences of chromosomal imbalance. Proc Natl Acad Sci USA. 1994;91(11):4997-5001.
  17. Vozdova M, Oracova E, Musilova P, Kasikova K, Prinosilova P, Gaillyova R, et al. Sperm and embryo analysis of similar t (7;10) translocations transmitted in two families. Fertil Steril. 2011;96(1):e66-70.
  18. Anton E, Vidal F, Blanco J. Reciprocal translocations: tracing their meiotic behavior. Genet Med. 2008;10(10):730-8.
  19. Fan J, Zhang X, Chen Y, Zhang J, Zhang L, Bi X, et al. Exploration of the interchromosomal effects in preimplantation genetic testing for structural rearrangements based on next‐generation sequencing. Mol Genet Genom Med. 2022;10(9):e2017.
  20. Gianaroli L, Magli M, Ferraretti A, Munne S, Balicchia B, Escudero T, et al. Possible interchromosomal effect in embryos generated by gametes from translocation carriers. Hum Reprod. 2002;17(12):3201-7.
  21. Van Hummelen P, Manchester D, Lowe X, Wyrobek AJ. Meiotic segregation, recombination, and gamete aneuploidy assessed in at (1;10)(p22.1;q22.3) reciprocal translocation carrier by three-and four-probe multicolor FISH in sperm. Am J Hum Genet. 1997;61(3):651-9.
  22. Blanco J, Egozcue J, Clusellas N, Vidal F. FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t (5;8)(q33;q13). Cytogenet Cell Genet. 1998;83(3-4):275-80.
  23. Acar H, Yildirim MS, Çora T, Ceylaner S. Evaluation of segregation patterns of 21; 21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH technique. Mol Reprod Dev. 2002;63(2):232-6.
  24. Hatakeyama C, Gao H, Harmer K, Ma S. Meiotic segregation patterns and ICSI pregnancy outcome of a rare (13;21) Robertsonian translocation carrier: a case report. Hum Reprod. 2006;21(4):976-9.
  25. Syme RM, Martin RH. Meiotic segregation of a 21;22 robertsonian translocation. Hum Reprod. 1992;7(6):825-9.
  26. Anton E, Vidal F, Blanco J. Interchromosomal effect analyses by sperm FISH: incidence and distribution among reorganization carriers. Syst Biol Reprod Med. 2011;57(6):268-78.
  27. Zhang S, Lei C, Wu J, Zhou J, Xiao M, Zhu S, et al. Meiotic heterogeneity of trivalent structure and interchromosomal effect in blastocysts with robertsonian translocations. Front Genet. 2021;12:609563.
  28. Guichaoua MR, Quack B, Speed RM, Noel B, Chandley AC, Luciani JM. Infertility in human males with autosomal translocations: meiotic study of a 14;22 robertsonian translocation. Hum Genet. 1990;86(2):162-6.