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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...

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Detalles Bibliográficos
Autores principales: Aydin, Çetin, Eris, Serenat, Yalcin, Yakup, Sen Selim, Halime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
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.
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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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