Literature DB >> 25433561

Cytogenetic abnormalities in Tunisian women with premature ovarian failure.

Wiem Ayed1, Ahlem Amouri2, Wajih Hammami1, Olfa Kilani1, Zinet Turki3, Fatma Harzallah4, Nouha Bouayed-Abdelmoula5, Imen Chemkhi6, Fethi Zhioua7, Claude Ben Slama3.   

Abstract

To identify the distribution of chromosome abnormalities among Tunisian women with premature ovarian failure (POF) referred to the department of Cytogenetic at the Pasteur Institute of Tunis (Tunisia), standard cytogenetic analysis was carried out in a total of 100 women younger than 40 affected with premature ovarian failure. We identified 18 chromosomal abnormalities, including seven X-numerical anomalies in mosaic and non-mosaic state (45,X; 47,XXX), four sex reversal, three X-structural abnormalities (terminal deletion and isochromosomes), one autosomal translocation and one supernumerary marker. The overall prevalence of chromosomal abnormalities was 18% in our cohort. X chromosome aneuploidy was the most frequent aberration. This finding confirms the essential role of X chromosome in ovarian function and underlies the importance of cytogenetic investigations in the routine management of POF.
Copyright © 2014 Académie des sciences. Published by Elsevier SAS. All rights reserved.

Entities:  

Keywords:  Amenorrhoea; Aménorrhée; Anomalies chromosomiques; Caryotype; Chromosome X; Insuffisance ovarienne prématurée; Karyotype; Premature ovarian failure; X Chromosome abnormalities

Mesh:

Substances:

Year:  2014        PMID: 25433561     DOI: 10.1016/j.crvi.2014.09.003

Source DB:  PubMed          Journal:  C R Biol        ISSN: 1631-0691            Impact factor:   1.583


  5 in total

Review 1.  Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.

Authors:  Nicole Tartaglia; Susan Howell; Shanlee Davis; Karen Kowal; Tanea Tanda; Mariah Brown; Cristina Boada; Amanda Alston; Leah Crawford; Talia Thompson; Sophie van Rijn; Rebecca Wilson; Jennifer Janusz; Judith Ross
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-07       Impact factor: 3.908

Review 2.  Genetics of primary ovarian insufficiency: new developments and opportunities.

Authors:  Yingying Qin; Xue Jiao; Joe Leigh Simpson; Zi-Jiang Chen
Journal:  Hum Reprod Update       Date:  2015-08-04       Impact factor: 15.610

3.  Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.

Authors:  Ayberk Turkyilmaz; Ceren Alavanda; Esra Arslan Ates; Bilgen Bilge Geckinli; Hamza Polat; Mehmet Gokcu; Taner Karakaya; Alper Han Cebi; Mehmet Ali Soylemez; Ahmet İlter Guney; Pinar Ata; Ahmet Arman
Journal:  J Assist Reprod Genet       Date:  2022-01-22       Impact factor: 3.357

4.  Cytogenetic Studies in Primary Amenorrhoea Cases.

Authors:  Elham Ghadirkhomi; Akram Ghdirkhomi; Seyed Abdolhamid Angaji
Journal:  J Hum Reprod Sci       Date:  2022-06-30

Review 5.  The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases.

Authors:  Hadeel T Zedan; Fatma H Ali; Hatem Zayed
Journal:  Chromosoma       Date:  2022-07-30       Impact factor: 2.919

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.