Literature DB >> 18230121

Double aneuploidy in a Turkish child: Down-Klinefelter syndrome.

Ali Karaman1, Eşref Kabalar.   

Abstract

The occurrence of double aneuploidy in the one person is a relatively rare phenomenon. A 5-year-old child, the second-born of non-consanguineous parents, possessed an extra X chromosome in addition to trisomy 21. The proband's parents and his brother showed normal karyotype. The phenotypic characteristics of the child have been discussed in light of the published reports on double aneuploidies of XXY and trisomy 21.

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Year:  2008        PMID: 18230121     DOI: 10.1111/j.1741-4520.2007.00174.x

Source DB:  PubMed          Journal:  Congenit Anom (Kyoto)        ISSN: 0914-3505            Impact factor:   1.409


  2 in total

1.  A Rare Double Aneuploidy Case (Down-Klinefelter).

Authors:  Sevcan Tug Bozdogan; Atil Bisgin
Journal:  J Pediatr Genet       Date:  2017-07-06

2.  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 in total

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