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Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family
Background: Approximately 205 million pregnancies occur each year in the worldwide. On the other hand, Spontaneous abortion has been reported in 15-20% of all diagnosed pregnancies. The most common cause of spontaneous abortion is chromosomal abnormalities of the embryo. Robertsonian translocation c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233318/ https://www.ncbi.nlm.nih.gov/pubmed/25408709 |
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author | Hasanzadeh-NazarAbadi, Mohammad Baghbani, Fatemeh Namazi, Iman Mirzaee, Salmeh |
author_facet | Hasanzadeh-NazarAbadi, Mohammad Baghbani, Fatemeh Namazi, Iman Mirzaee, Salmeh |
author_sort | Hasanzadeh-NazarAbadi, Mohammad |
collection | PubMed |
description | Background: Approximately 205 million pregnancies occur each year in the worldwide. On the other hand, Spontaneous abortion has been reported in 15-20% of all diagnosed pregnancies. The most common cause of spontaneous abortion is chromosomal abnormalities of the embryo. Robertsonian translocation carriers specially 21-14 are the most common balanced rearrangement among the carrier couples with the history of spontaneous abortion. In order to search for balanced chromosomal rearrangement and cytogenetic disorders, 10 members of related family with consanguinity marriage with the history of recurrent miscarriage were assessed. Case: Cytogenetic evaluation on the basis G-banding technique at high resolution was performed in 3 couples and their related family with the history of idiopathic RSA in order to postulate any balanced chromosomal rearrangement. Conclusion: six members of them appeared with robertsonian balanced translocation between chromosome No.21 to No. 14 with the karyotype of 45, XX, t (14, 21) and 45, XY, t (14, 21), which this results are in agreement with several similar works which claimed that the risk of spontaneous abortion in couples with balanced chromosomal rearrangements is higher compared with general population. Considering to results of present study, it seems as if the cytogenetic analysis of couples with the history of recurrent abortions should be suggested compulsory to estimate the probable presence of any chromosomal rearrangement. This offer wills valuable information for genetic consulting. |
format | Online Article Text |
id | pubmed-4233318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Research and Clinical Center for Infertility |
record_format | MEDLINE/PubMed |
spelling | pubmed-42333182014-11-18 Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family Hasanzadeh-NazarAbadi, Mohammad Baghbani, Fatemeh Namazi, Iman Mirzaee, Salmeh Iran J Reprod Med Case Report Background: Approximately 205 million pregnancies occur each year in the worldwide. On the other hand, Spontaneous abortion has been reported in 15-20% of all diagnosed pregnancies. The most common cause of spontaneous abortion is chromosomal abnormalities of the embryo. Robertsonian translocation carriers specially 21-14 are the most common balanced rearrangement among the carrier couples with the history of spontaneous abortion. In order to search for balanced chromosomal rearrangement and cytogenetic disorders, 10 members of related family with consanguinity marriage with the history of recurrent miscarriage were assessed. Case: Cytogenetic evaluation on the basis G-banding technique at high resolution was performed in 3 couples and their related family with the history of idiopathic RSA in order to postulate any balanced chromosomal rearrangement. Conclusion: six members of them appeared with robertsonian balanced translocation between chromosome No.21 to No. 14 with the karyotype of 45, XX, t (14, 21) and 45, XY, t (14, 21), which this results are in agreement with several similar works which claimed that the risk of spontaneous abortion in couples with balanced chromosomal rearrangements is higher compared with general population. Considering to results of present study, it seems as if the cytogenetic analysis of couples with the history of recurrent abortions should be suggested compulsory to estimate the probable presence of any chromosomal rearrangement. This offer wills valuable information for genetic consulting. Research and Clinical Center for Infertility 2014-08 /pmc/articles/PMC4233318/ /pubmed/25408709 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Hasanzadeh-NazarAbadi, Mohammad Baghbani, Fatemeh Namazi, Iman Mirzaee, Salmeh Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title | Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title_full | Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title_fullStr | Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title_full_unstemmed | Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title_short | Robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
title_sort | robertsonian translocation between chromosomes (no.21/14) in relation to the history of spontaneous abortion in a family |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233318/ https://www.ncbi.nlm.nih.gov/pubmed/25408709 |
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