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An Interesting Prenatal Diagnosis: Double Aneuploidy
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 d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867918/ https://www.ncbi.nlm.nih.gov/pubmed/24368953 http://dx.doi.org/10.1155/2013/790286 |
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author | Aydin, Çetin Eris, Serenat Yalcin, Yakup Sen Selim, Halime |
author_facet | Aydin, Çetin Eris, Serenat Yalcin, Yakup Sen Selim, Halime |
author_sort | Aydin, Çetin |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3867918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38679182013-12-24 An Interesting Prenatal Diagnosis: Double Aneuploidy Aydin, Çetin Eris, Serenat Yalcin, Yakup Sen Selim, Halime Case Rep Obstet Gynecol Case Report 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. Hindawi Publishing Corporation 2013 2013-12-04 /pmc/articles/PMC3867918/ /pubmed/24368953 http://dx.doi.org/10.1155/2013/790286 Text en Copyright © 2013 Çetin Aydin et al. https://creativecommons.org/licenses/by/3.0/ 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. |
spellingShingle | Case Report Aydin, Çetin Eris, Serenat Yalcin, Yakup Sen Selim, Halime An Interesting Prenatal Diagnosis: Double Aneuploidy |
title | An Interesting Prenatal Diagnosis: Double Aneuploidy |
title_full | An Interesting Prenatal Diagnosis: Double Aneuploidy |
title_fullStr | An Interesting Prenatal Diagnosis: Double Aneuploidy |
title_full_unstemmed | An Interesting Prenatal Diagnosis: Double Aneuploidy |
title_short | An Interesting Prenatal Diagnosis: Double Aneuploidy |
title_sort | interesting prenatal diagnosis: double aneuploidy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867918/ https://www.ncbi.nlm.nih.gov/pubmed/24368953 http://dx.doi.org/10.1155/2013/790286 |
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