| Literature DB >> 25433561 |
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.Entities:
Keywords: Amenorrhoea; Aménorrhée; Anomalies chromosomiques; Caryotype; Chromosome X; Insuffisance ovarienne prématurée; Karyotype; Premature ovarian failure; X Chromosome abnormalities
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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