Jul 2026· Journal of reproduction & infertility· Vol 27, pp. 75 - 79· 0 citations· 29 references
Medicine
TL;DR
Prenatal screening for carriers of ROBs is strongly recommended to assess the risk of unbalanced chromosomal disorders in offspring and the role of t(13;14) and ICE as potential contributors to the birth of a child with DS was explored.
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.
Mosaicism for both a ring chromosome and Robertsonian translocation is a rarely reported cytogenetic phenomenon. We describe a case referred for testing following abnormal noninvasive prenatal screening for trisomy 13. Prenatal chromosomal microarray (CMA) testing identified a mosaic 3.6‐Mb terminal loss in 13q34, whic...
Katherine M. Haines, Deborah M. Hazard, Billie Carstens et al.· Case Reports in Genetics· 0 citations
This first case with these alterations in the same patient demonstrates the importance of complementary analytical techniques and the ideal future goal of routinely implementing simultaneous genetic analyses with complementary tests to improve the understanding of the genome and its potential alterations.
Background:
Heterochromatin variants of chromosome Y (Yqh+) are classified by international cytogenetic nomenclature as benign polymorphisms. However, several case-control studies have reported a higher frequency of these variants among couples with recurrent pregnancy loss, and a plausible sex-specific mechanism ha...
Omer I. Aljumaili, A. Ahmed, Ibtisam T. S. Al Aboosi· BIO Web of Conferences· 0 citations
Recombinant chromosome 8, rec(8) is associated with a syndrome, often reported in individuals of Hispanic ancestry, characterized by moderate-to-severe intellectual disability, craniofacial dysmorphism, and congenital heart or urogenital anomalies. It typically results from a parental pericentric inversion on chromos...
S. Agarwal, M. Lall, S. Bijarnia-Mahay et al.· Genetic clinics· 0 citations
46,XX testicular disorder of sex development (DSD), also known as XX male syndrome, is a rare condition where an individual with a 46,XX karyotype develops a male phenotype. In 90% of cases, the syndrome results from the translocation of the
SRY
gene to the X chromosome or an autosome. The remaining 10% of individu...
Júlia Martinková, Hana Řezáčová, A. Šantavá et al.· Frontiers in Genetics· 0 citations
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