Objective: To investigate the pregnancy outcomes of couples with either maternal or paternal balanced translocations.
Methods: One hundred and ninety-four couples were divided into three groups based on the kind of translocations: 135 with reciprocal translocation, 52 with nonhomologous Robertsonian translocations, and 7 with homologous Robertsonian translocations. Past reproductive histories were surveyed. For those who wanted to have their own babies by natural conceptions after knowing their karyotypes as well as the risks of abnormal offsprings, subsequent pregnancy outcomes were recorded. Total pregnancy outcomes were compared between three groups.
Results: (1) 503 previous and subsequent pregnancies were recorded in detail. The pregnancy outcomes are as follows: spontaneous abortions 81.7% (411/503); induced terminations because of fetal abnormalities 3.2% (16/503); birth defects 7.2% (36/503); normal/balanced offsprings 8.0% (40/503). In reciprocal translocations, nonhomologous Robertsonian translocations and homologous Robertsonian translocations, the birth defects rates were 5.7% (20/350), 10.9% (14/128) and 8.0% (2/25), respectively (P < 0.05). The rates of normal/balanced offsprings in each group were 6.6% (23/350), 13.28% (17/128) and 0, respectively (P < 0.05). The rates of spontaneous abortions as well as the rates of induced terminations among three groups had no statistical differences. (2) Among the 52 congenital defects, induced terminations accounted for 30.8% (16/52), and liveborn 69% (36/52). Cytogenetic analyses were performed for 27 congenital defects and Down's syndrome occupied 59% (16/27). (3) 39 couples with reciprocal or nonhomologous Robertsonian translocations gave birth to 40 normal/balanced offsprings, of which 26 were karyotyped: normal karyotypes were 6 (23%) and balanced translocations 20 (77%). Couples with homologous Robertsonian translocations had no normal/balanced offspring.
Conclusions: Balanced translocation carriers suffer from poor pregnancy prognosis. Couples with homologous Robertsonian translocations have little chance to give birth to normal/balanced offsprings.
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Mol Genet Genomic Med
January 2025
Center of Reproductive Medicine, Affiliated Children's Hospital of Shanxi & Women Health Center of Shanxi Medicine University, Taiyuan, Shanxi, China.
Introduction: This study investigated the impact of the carrier on transferable blastocyst rate and live birth outcomes in couples with structural chromosomal abnormalities.
Methods: Couples were grouped into reciprocal translocation, Robertsonian translocation, or inversions groups, and clinical data were retrospectively analyzed. Preimplantation genetic testing for chromosomal structural rearrangements (PGT-SR) was conducted, and pregnancy outcomes were compared.
Theor Appl Genet
December 2024
Hungarian Research Network (HUN-REN), Centre for Agricultural Research, Agricultural Institute, Martonvásár, 2462, Hungary.
GBS read coverage analysis identified a Robertsonian chromosome from two Thinopyrum subgenomes in wheat, conferring leaf and stripe rust resistance, drought tolerance, and maintaining yield stability. Agropyron glael (GLAEL), a Thinopyrum intermedium × Th. ponticum hybrid, serves as a valuable genetic resource for wheat improvement.
View Article and Find Full Text PDFMedicina (Kaunas)
October 2024
Laboratory of Human Genomics, University of Medicine and Pharmacy of Craiova, 200638 Craiova, Romania.
Recurrent pregnancy loss (RPL) is a multifactorial condition, encompassing genetic, anatomical, immunological, endocrine, as well as infectious and environmental factors; however, the etiology remains elusive in a substantial number of cases. Genetic factors linked to RPL include parental karyotype abnormalities (e.g.
View Article and Find Full Text PDFFertil Steril
November 2024
Instituto Valenciano de Infertilidad and Reproductive Medicine Associates Global Research Alliance, Reproductive Medicine Associates of New Jersey, Basking Ridge, New Jersey.
Am J Hum Genet
December 2024
Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02115, USA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. Electronic address:
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