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Case Reports in Obstetrics and GynecologyVolume 2013 2013, Article ID 790286, 3 pages

Case Report

Gynecology and Obstetrics Department of Ataturk Training and Research Hospital, Basin Sitesi, Yesilyurt, 35360 Izmir, Turkey

Gynecology and Obstetrics Department of Van Training and Research Hospital, Süphan Street, 65300 Van, Turkey

Received 7 August 2013; Accepted 5 October 2013

Academic Editors: A. Ohkuchi and A. Semczuk

Copyright © 2013 Çetin Aydin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Double aneuploidy, the existence of two chromosomal abnormalities in the same individual, is a rare condition. Early diagnosis of this condition is important to offer termination of pregnancy in genetic counselling. Cytogenetic analysis with amniocentesis and ultrasound examination is valuable for diagnosis of double aneuploidy. In this report we present a case with the karyotype of 48XXY+21 diagnosed prenatally.

Autor: Çetin Aydin, Serenat Eris, Yakup Yalcin, and Halime Sen Selim



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