Literature DB >> 18564502

A male case with double aneuploidy (48,XXY,+21).

E Akbas1, F Soylemez, K Savasoglu, O Halliogluand, S Balci.   

Abstract

The co-occurrence of two numerical chromosomal abnormalities in same individual (double aneuploidy) is relatively rare and the clinical presentations are variable depending on the predominating aneuploidy or a combination effect of both. Furthermore, double aneuploidy involving both autosomal and sex chromosomes is seldom described. We describe a male patient with typical clinical features of Down Syndrome and his karyotype revealed 48,XXY,+21. The phenotypic characteristics of this child have been discussed in the light of the published reports on double aneuploidies of XXY and trisomy 21.

Entities:  

Mesh:

Year:  2008        PMID: 18564502

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  3 in total

1.  Down-Klinefelter Syndrome (48,XXY,+21) in a Saudi Neonate: A Case Report and Literature Review.

Authors:  Jubara Alallah; Sohaib Habhab; Farzeen Mohtisham; Aiman Shawli; Mustafa Daghistani
Journal:  Cureus       Date:  2022-04-28

2.  Double aortic arch with double aneuploidy--rare anomaly in combined Down and Klinefelter syndrome.

Authors:  Maaike F Gerretsen; Willem Peelen; Lukas A J Rammeloo; David R Koolbergen; Jaroslav Hruda
Journal:  Eur J Pediatr       Date:  2009-03-05       Impact factor: 3.183

3.  Double Aneuploidy 48,XXY,+21 Associated with a Congenital Heart Defect in a Neonate.

Authors:  X Shu; C Zou; Z Shen
Journal:  Balkan J Med Genet       Date:  2013-12       Impact factor: 0.519

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.