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Although karyotyping technology has been implemented in genetic diagnosis for a long time, the comprehensive understanding of this technology is still limited. The aim of this study was to investigate the accuracy and resolution of karyotyping method in detecting chromosomal abnormalities by molecular genetic method. In this study, we conducted a retrospective analysis of embryonic molecular karyotypes and peripheral blood cytogenetic karyotypes from patients with balanced chromosomal rearrangements undergoing preimplantation genetic testing at our reproductive center. Blood karyotyping was performed using routine G-banding at the 400-band resolution by two well-trained technicians. The embryonic molecular karyotypes were detected using either high-throughput sequencing or single nucleotide polymorphism microarray method. We compared the breakpoint locations, determined by unbalanced rearrangements, in the embryonic molecular karyotypes with the corresponding rearranged chromosome bands in the peripheral blood karyotypes. A total of 508 cases were enrolled and 2078 embryos were detected, 404 cases were analyzed finally. We found that only 39.32% (289/735) of embryonic molecular breakpoints were located within the rearranged bands identified by peripheral blood karyotyping, while the remaining 60.68% (446/735) fell outside these regions. Our results showed only 73 cases exhibited accurate karyotyping results, indicating an accuracy rate of 18.07%. Furthermore, the average resolution of karyotyping technique was found to be approximately 9.01 megabases (Mb) pairs. These findings provide profound insight into the accuracy and resolution of karyotyping techniques, which can contribute to more precise genetic counseling.
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http://dx.doi.org/10.1007/s00438-025-02282-2 | DOI Listing |
Eur J Obstet Gynecol Reprod Biol
August 2025
Reproductive Medicine Center, Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen 518000 Guangdong, China; Shenzhen Clinical Research Center for Obstetrics & Gynecology and Reproductive System Diseases, Shenzhen 518000 Guangdong, China. Electronic address: szfyart
Objective: This study investigates the association between alobar holoprosencephaly (HPE) and de novo germline microdeletions in the Xq25 region. To develop a Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) based workflow enabling high-resolution preimplantation detection of sub-Mb microdeletions, overcoming the >1 Mb resolution limit of conventional whole genome amplification(WGA) copy number variation(CNV) sequencing to identify causative Xq25 variants and prevent pathogenic microdeletion transmission.
Methods: This study presents a clinical case involving a couple with an adverse obstetric history accompanied by two occurrences of HPE.
DNA abnormalities characterized by cytogenetic imaging at the single cell resolution, i.e. karyotyping, have long served as cancer diagnostic and prognostic biomarkers.
View Article and Find Full Text PDFFront Genet
August 2025
Prenatal Diagnostic Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Healthcare Hospital, Beijing, China.
Background: Chromosomal karyotype analysis remains a classical and frontline method in prenatal diagnosis, capable of detecting balanced chromosomal abnormalities and providing insights distinct from high-resolution molecular techniques such as CMA and CNV-Seq. However, large-scale studies on the distribution of structural abnormalities and mosaicism in amniotic fluid karyotypes are scarce, with most previous research focusing on common aneuploidies.
Objective: The study aimed to elucidate the relationship between chromosomal structural abnormalities and specific chromosomes.
Methods Mol Biol
August 2025
Division of Hematology, Oncology, and Cancer Immunology, Medical Department, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Structural variants are of major importance in cancer genetics. Especially when it comes to the detection of complex structural variants as in chromoanagenesis, detection tools like array-CGH, karyotyping, or even whole-genome sequencing do not provide the necessary resolution and/or accuracy. Here, we present a novel structural variant (SV) detection workflow that integrates genomic DNA (gDNA) long-read sequencing and Hi-C sequencing.
View Article and Find Full Text PDFGenes (Basel)
August 2025
Department of Obstetrics and Gynaecology, Podobnik Special Hospital, Ul. Sveti Duh 112, 10000 Zagreb, Croatia.
Background/objectives: Cystic hygroma is a congenital lymphatic malformation often identified during early pregnancy and frequently associated with chromosomal abnormalities and adverse outcomes. We aimed to appraise the genetic and clinical characteristics of fetuses diagnosed with cystic hygroma in the first/early second trimester, assess the resolution patterns in chromosomally normal cases, and provide insights into prognosis-based on data collected over a 30-year period.
Methods: A retrospective cohort study was conducted on 405 consecutive fetuses diagnosed with nuchal cystic hygroma between 8.