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Pericentric inversion in chromosome 1 and male infertility

Pericentric inversion in chromosome 1 was thought to cause male infertility through spermatogenic impairment, regardless of the breakpoint position. However, carriers of pericentric inversion in chromosome 1 have been reported with normal fertility and familial transmission. Here, we report two case...

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Detalles Bibliográficos
Autores principales: Li, Ranwei, Fan, Haitao, Zhang, Qiushuang, Yang, Xiao, Zhan, Peng, Feng, Shuqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712408/
https://www.ncbi.nlm.nih.gov/pubmed/33335995
http://dx.doi.org/10.1515/med-2020-0404
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author Li, Ranwei
Fan, Haitao
Zhang, Qiushuang
Yang, Xiao
Zhan, Peng
Feng, Shuqiang
author_facet Li, Ranwei
Fan, Haitao
Zhang, Qiushuang
Yang, Xiao
Zhan, Peng
Feng, Shuqiang
author_sort Li, Ranwei
collection PubMed
description Pericentric inversion in chromosome 1 was thought to cause male infertility through spermatogenic impairment, regardless of the breakpoint position. However, carriers of pericentric inversion in chromosome 1 have been reported with normal fertility and familial transmission. Here, we report two cases of pericentric inversion in chromosome 1. One case was detected in utero via amniocentesis, and the other case was detected after the wife of the carrier experienced two spontaneous abortions within 5 years of marriage. Here, the effect of the breakpoint position of the inversion in chromosome 1 on male infertility is examined and compared with the published cases. The association between the breakpoint of pericentric inversion in chromosome 1 and spermatogenesis is also discussed. Overall, the results suggest that the breakpoint position deserves attention from physicians in genetic counseling as inversion carriers can produce offspring.
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spelling pubmed-77124082020-12-16 Pericentric inversion in chromosome 1 and male infertility Li, Ranwei Fan, Haitao Zhang, Qiushuang Yang, Xiao Zhan, Peng Feng, Shuqiang Open Med (Wars) Research Article Pericentric inversion in chromosome 1 was thought to cause male infertility through spermatogenic impairment, regardless of the breakpoint position. However, carriers of pericentric inversion in chromosome 1 have been reported with normal fertility and familial transmission. Here, we report two cases of pericentric inversion in chromosome 1. One case was detected in utero via amniocentesis, and the other case was detected after the wife of the carrier experienced two spontaneous abortions within 5 years of marriage. Here, the effect of the breakpoint position of the inversion in chromosome 1 on male infertility is examined and compared with the published cases. The association between the breakpoint of pericentric inversion in chromosome 1 and spermatogenesis is also discussed. Overall, the results suggest that the breakpoint position deserves attention from physicians in genetic counseling as inversion carriers can produce offspring. De Gruyter 2020-04-20 /pmc/articles/PMC7712408/ /pubmed/33335995 http://dx.doi.org/10.1515/med-2020-0404 Text en © 2020 Ranwei Li et al., published by De Gruyter http://creativecommons.org/licenses/by/4.0 This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Li, Ranwei
Fan, Haitao
Zhang, Qiushuang
Yang, Xiao
Zhan, Peng
Feng, Shuqiang
Pericentric inversion in chromosome 1 and male infertility
title Pericentric inversion in chromosome 1 and male infertility
title_full Pericentric inversion in chromosome 1 and male infertility
title_fullStr Pericentric inversion in chromosome 1 and male infertility
title_full_unstemmed Pericentric inversion in chromosome 1 and male infertility
title_short Pericentric inversion in chromosome 1 and male infertility
title_sort pericentric inversion in chromosome 1 and male infertility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712408/
https://www.ncbi.nlm.nih.gov/pubmed/33335995
http://dx.doi.org/10.1515/med-2020-0404
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