A Rare Double Aneuploidy with 48,XXY, +21 Karyotype in Down Syndrome from Gujarat, India  

Pankaj K. Gadhia , Salil N. Vaniawala
Molecular Cytogenetic Unit, S. N. Gene Lab. and Research Centre, President Plaza-A, Near RTO circle, Surat, India
Author    Correspondence author
International Journal of Molecular Medical Science, 2014, Vol. 4, No. 4   doi: 10.5376/ijmms.2014.04.0004
Received: 31 Oct., 2014    Accepted: 18 Nov., 2014    Published: 23 Dec., 2014
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Preferred citation for this article:

Gadhia and Vaniawala, 2014, A Rare Double Aneuploidy with 48,XXY, +21 Karyotype in Down Syndrome from Gujarat, India, International Journal of Molecular Medical Science, Vol.4, No.4, 1-3 (doi: 10.5376/ijmms.2014.04.0004)
 

Abstract

The occurrence of double aneuploidy in single individual is relatively rare phenomenon. A 12 – month old child has an extra X chromosome in addition to trisomy 21. The phenotypic characteristics of child were similar to Down syndrome. Cytogenetic finding revealed 48,XXY, +21 karyotype. Results have been discussed in light of published case reports on double aneuploidies of XXY, +21.

Keywords
Double aneuploidy; Down syndrome; Klinfelter syndrome; Gujarat; India
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