Literature DB >> 20666944

Are heterochromatin polymorphisms associated with recurrent miscarriage?

Ahmet Okay Caglayan1, Isilay Ozyazgan, Fatma Demiryilmaz, Mahmut Tuncay Ozgun.   

Abstract

AIM: Recurrent miscarriage is a multifactorial problem associated with genetic abnormalities reflected by inherited disorders. The aim of the present study was to investigate the contribution of chromosomal abnormalities and the frequency of a particular type of aberration in couples of Turkish origin with recurrent miscarriages compared with patients without miscarriages.
METHODS: A total of 336 patients with recurrent miscarriages and 427 patients without miscarriages were analyzed.
RESULTS: In the recurrent miscarriage group, a structural chromosomal abnormality was found in four patients (1%). Twelve patients had mosaic karyotype (3%) and the total rate of chromosomal abnormalities was 4% in this group. The karyotypes were composed of polymorphisms in 8% of patients with recurrent miscarriages compared with 4% in the control group (P < 0.05).
CONCLUSION: The overall high incidence of chromosome polymorphisms in patients with recurrent miscarriages compared to the normal population needs to be confirmed with additional investigations including larger populations in order to delineate the role of 'harmless' chromosomal aberrations in the etiology of recurrent spontaneous abortions.

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Year:  2010        PMID: 20666944     DOI: 10.1111/j.1447-0756.2010.01207.x

Source DB:  PubMed          Journal:  J Obstet Gynaecol Res        ISSN: 1341-8076            Impact factor:   1.730


  11 in total

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4.  [Chromosomal polymorphisms are associated with blastomere multinucleation in IVF/ICSI cycles].

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5.  Chromosomal polymorphisms involved in reproductive failure in the romanian population.

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6.  Cytogenetic results of patients with infertility in middle anatolia, Turkey: do heterochromatin polymorphisms affect fertility?

Authors:  Caglayan Ahmet Okay; Ozyazgan Isilay; Demiryilmaz Fatma; Dundar Munis
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7.  Y chromosome polymorphisms may contribute to an increased risk of male-induced unexplained recurrent miscarriage.

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Journal:  Biosci Rep       Date:  2017-03-27       Impact factor: 3.840

8.  A Case-Control Study Identifying the Frequency and Spectrum of Chromosomal Anomalies and Variants in a Cohort of 1000 Couples with a Known History of Recurrent Pregnancy Loss in the Eastern Region of India.

Authors:  Abhik Chakraborty; Sujata Kar; Purna Chandra Mohapatra; Birendranath Banerjee
Journal:  J Hum Reprod Sci       Date:  2021-12-31

9.  A homozygous NOP14 variant is likely to cause recurrent pregnancy loss.

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10.  The synergic effects of CTLA-4/Foxp3-related genotypes and chromosomal aberrations on the risk of recurrent spontaneous abortion among a Chinese Han population.

Authors:  Qin'e Fan; Juanjuan Zhang; Yu Cui; Chaoyun Wang; Yongjun Xie; Qiurong Wang; Libing Wu
Journal:  J Hum Genet       Date:  2018-02-23       Impact factor: 3.172

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