Literature DB >> 15050879

Double trisomy (48,XXY,+21) in monozygotic twins: case report and review of the literature.

Dimitrios Iliopoulos1, George Poultsides, Vasiliki Peristeri, Georgia Kouri, Alexandros Andreou, Nikolaos Voyiatzis.   

Abstract

The occurrence of double aneuploidy in the same individual is a relatively rare phenomenon. We describe twin newborns with typical clinical features of Down's syndrome, of which one revealed 48,XXY,+21 GTG-band karyotype. The second newborn died 2 days after its birth, and was clinically diagnosed having Down syndrome. Due to the same clinical features of the twins, the common placenta and amniotic sac, we speculate that they were monozygotics and as a result the second newborn should also be a Klinefelter. The purpose of this report is to present a rare case of possible coincidence of double aneuploidy in newborn twins. A review of the literature showed that double trisomy (48,XXY,+21) in a twin newborn infant has never occurred.

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Year:  2004        PMID: 15050879     DOI: 10.1016/j.anngen.2003.08.025

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  6 in total

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

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

Review 2.  Clinical and hormonal status of infants with nonmosaic XXY karyotype.

Authors:  Najiba Lahlou; Ilene Fennoy; Judith L Ross; Claire Bouvattier; Marc Roger
Journal:  Acta Paediatr       Date:  2011-04-20       Impact factor: 2.299

3.  Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype.

Authors:  Laura Daniela Vergara-Mendez; Claudia Talero-Gutiérrez; Alberto Velez-Van-Meerbeke
Journal:  J Genet       Date:  2018-03       Impact factor: 1.166

4.  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

Review 5.  What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature.

Authors:  Eva Pinti; Anna Lengyel; Gyorgy Fekete; Iren Haltrich
Journal:  BMC Pediatr       Date:  2020-01-13       Impact factor: 2.125

6.  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

  6 in total

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