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Premature ovarian failure and 46,X,del(X)(q21)

Date

2012

Author

Kara N.
Tural Ş.
Okten G.
Kocak I.
Tekcan A.

Metadata

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Abstract

Premature ovarian failure (POF) is a common cause of infertility in women, and is characterised by amenorrhoea, hypo-oestrogenism and elevated gonadotrophin levels in women under the age of 40. Genetic, autoimmune and the environmental factors play a role in the pathogenesis. In this study, we investigated a 22 year-old woman having premature ovarian failure, referred to our laboratuary from Ondokuz Mayis University Gynecology and Obstetrics polyclinic. In conventional cytogenetic analysis, a deletion was observed in the long arm of the X chromosome 46,X,del(X)(q21). This finding was emphasised once again the significance of X chromosome deletions in the premature ovarian failure. © 2012 OMU.

Source

Ondokuz Mayis Universitesi Tip Dergisi

Volume

29

Issue

2

URI

https://doi.org/10.5835/jecm.omu.29.02.018
https://hdl.handle.net/20.500.12712/4449

Collections

  • Scopus İndeksli Yayınlar Koleksiyonu [14046]



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