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Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports
BACKGROUND: Recurrent spontaneous abortion (RSA) is often idiopathic, but structural chromosomal abnormality is an important nosogenesis. Balanced translocations or inversions can lead to unbalanced gametes depending on the specific recombination and segregation patterns during meiosis. An unbalance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142492/ https://www.ncbi.nlm.nih.gov/pubmed/34024271 http://dx.doi.org/10.1186/s13256-021-02848-9 |
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author | Wan, Xue Li, Linyan Liu, Zulin Fan, Zhenhai Yu, Limei |
author_facet | Wan, Xue Li, Linyan Liu, Zulin Fan, Zhenhai Yu, Limei |
author_sort | Wan, Xue |
collection | PubMed |
description | BACKGROUND: Recurrent spontaneous abortion (RSA) is often idiopathic, but structural chromosomal abnormality is an important nosogenesis. Balanced translocations or inversions can lead to unbalanced gametes depending on the specific recombination and segregation patterns during meiosis. An unbalanced karyotype in the conceptus of a couple when one partner has a structural chromosomal abnormality may result in failure to implant, miscarriage, or ongoing pregnancy of a fetus with an unbalanced karyotype. CASE PRESENTATION: We report two rare Han cases of RSA associated with balanced translocation of chromosomes. In case 1, a women who had had four spontaneous abortions, the karyotype was 46, XX, t (4;7) (q31;q22). In case 2, a women who had two spontaneous abortions and one stillborn fetus, the karyotype was 46, XX, t (3;15) (q12;p11.2), inv (5) (P13q13). The abnormal karyotype was not found in other chromosomes. CONCLUSIONS: It is very important that couples with more than two miscarriages be provided with chromosomal analysis. Referring couples for karyotyping will rule out or confirm possible hereditary etiology and the source of chromosomal abnormalities in recurrent miscarriages. |
format | Online Article Text |
id | pubmed-8142492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81424922021-05-25 Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports Wan, Xue Li, Linyan Liu, Zulin Fan, Zhenhai Yu, Limei J Med Case Rep Case Report BACKGROUND: Recurrent spontaneous abortion (RSA) is often idiopathic, but structural chromosomal abnormality is an important nosogenesis. Balanced translocations or inversions can lead to unbalanced gametes depending on the specific recombination and segregation patterns during meiosis. An unbalanced karyotype in the conceptus of a couple when one partner has a structural chromosomal abnormality may result in failure to implant, miscarriage, or ongoing pregnancy of a fetus with an unbalanced karyotype. CASE PRESENTATION: We report two rare Han cases of RSA associated with balanced translocation of chromosomes. In case 1, a women who had had four spontaneous abortions, the karyotype was 46, XX, t (4;7) (q31;q22). In case 2, a women who had two spontaneous abortions and one stillborn fetus, the karyotype was 46, XX, t (3;15) (q12;p11.2), inv (5) (P13q13). The abnormal karyotype was not found in other chromosomes. CONCLUSIONS: It is very important that couples with more than two miscarriages be provided with chromosomal analysis. Referring couples for karyotyping will rule out or confirm possible hereditary etiology and the source of chromosomal abnormalities in recurrent miscarriages. BioMed Central 2021-05-24 /pmc/articles/PMC8142492/ /pubmed/34024271 http://dx.doi.org/10.1186/s13256-021-02848-9 Text en © The Author(s) 2021, corrected publication [2021] https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Wan, Xue Li, Linyan Liu, Zulin Fan, Zhenhai Yu, Limei Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title | Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title_full | Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title_fullStr | Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title_full_unstemmed | Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title_short | Recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
title_sort | recurrent spontaneous abortion related to balanced translocation of chromosomes: two case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142492/ https://www.ncbi.nlm.nih.gov/pubmed/34024271 http://dx.doi.org/10.1186/s13256-021-02848-9 |
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