Literature DB >> 18461436

Chromosome heteromorphisms: an impact on infertility.

Feride Iffet Sahin1, Zerrin Yilmaz, Ozge Ozalp Yuregir, Tugce Bulakbasi, Ozge Ozer, Hulusi Bulent Zeyneloglu.   

Abstract

INTRODUCTION: Cytogenetic heteromorphisms are described as heritable variations at specific chromosomal regions without a proven impact on phenotype.
MATERIALS AND METHODS: We compared the presence of chromosome heteromorphisms in the karyotypes of two patient groups. The first group of patients consisted of 276 individuals of 138 infertile couples. The second group, consisted of 1,130 amniocentesis samples. This group was considered to be a sample of the fertile population, as the fetus being karyotyped is the result of a spontaneous pregnancy. Fetal karyotyping was made due to the standard indications for prenatal diagnosis, such as abnormal maternal serum screening results. RESULTS AND DISCUSSION: Eighteen infertile patients (6.52%) and twenty fetuses (1.77%) were found to have chromosome heteromorphisms. The difference between the two groups was statistically significant (p < 0.0001).
CONCLUSION: These results are consistent with other similar studies that suggest the yet undefined relationship between chromosome heteromorphisms and infertility.

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Mesh:

Year:  2008        PMID: 18461436      PMCID: PMC2582066          DOI: 10.1007/s10815-008-9216-3

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  12 in total

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Review 2.  The genetic basis of infertility.

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Journal:  Reproduction       Date:  2003-07       Impact factor: 3.906

3.  Is there a possible correlation between chromosomal variants and spermatogenesis?

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Journal:  Int J Urol       Date:  2005-11       Impact factor: 3.369

4.  Characterization of human chromosomal constitutive heterochromatin.

Authors:  A Babu; R S Verma
Journal:  Can J Genet Cytol       Date:  1986-10

Review 5.  Polymorphic variants on chromosomes probably play a significant role in infertility.

Authors:  Prochi F Madon; Arundhati S Athalye; Firuza R Parikh
Journal:  Reprod Biomed Online       Date:  2005-12       Impact factor: 3.828

6.  A new approach in recognition of heterochromatic regions of human chromosomes by means of restriction endonucleases.

Authors:  A Babu; A K Agarwal; R S Verma
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

7.  Chromosomal variants among 1790 infertile men.

Authors:  Y Nakamura; M Kitamura; K Nishimura; M Koga; N Kondoh; M Takeyama; K Matsumiya; A Okuyama
Journal:  Int J Urol       Date:  2001-02       Impact factor: 3.369

8.  Cytogenetic analyses in infertile men.

Authors:  J Lissitsina; R Mikelsaar; M Punab
Journal:  Arch Androl       Date:  2006 Mar-Apr

Review 9.  Chromosomal abnormalities in couples undergoing intracytoplasmic sperm injection. A study of 370 couples and review of the literature.

Authors:  F Morel; N Douet-Guilbert; M-J Le Bris; V Amice; M T Le Martelot; S Roche; A Valéri; V Derrien; J Amice; M De Braekeleer
Journal:  Int J Androl       Date:  2004-06

10.  Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes.

Authors:  M Codina-Pascual; J Navarro; M Oliver-Bonet; J Kraus; M R Speicher; O Arango; J Egozcue; J Benet
Journal:  Hum Reprod       Date:  2006-02-16       Impact factor: 6.918

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  26 in total

1.  Reproductive success of assisted reproductive technology in couples with chromosomal abnormalities.

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Review 2.  Consensus statement on diagnosis and clinical management of Klinefelter syndrome.

Authors:  A F Radicioni; A Ferlin; G Balercia; D Pasquali; L Vignozzi; M Maggi; C Foresta; A Lenzi
Journal:  J Endocrinol Invest       Date:  2010-12       Impact factor: 4.256

3.  A novel chromosomal translocation and heteromorphism in a female with recurrent pregnancy loss--a case study.

Authors:  Venkateshwari Ananthapur; Srilekha Avvari; Vinod Cingeetham; Sujatha Maddireddi; Pratibha Nallari; Jyothy Akka
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4.  Long Y chromosome is not a fetal loss risk.

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5.  Male chromosomal polymorphisms reduce cumulative live birth rate for IVF couples.

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6.  Chromosomal aberrations and polymorphic evaluation in males with primary infertility from Indian population.

Authors:  Ushang V Kate; Yamini S Pokale; Ajinkya M Jadhav; Suresh D Gangane
Journal:  J Clin Diagn Res       Date:  2014-10-20

7.  Karyotype analysis in large-sample infertile couples living in Central China: a study of 14965 couples.

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8.  The effect of chromosomal polymorphisms on the outcomes of fresh IVF/ICSI-ET cycles in a Chinese population.

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

Authors:  Zhiheng Chen; Li Yang; Cuiqing Yi; Jun Liu; Ling Sun
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2020-01-30

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

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Journal:  J Hum Genet       Date:  2018-02-13       Impact factor: 3.172

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