Molecular Cytogenetics (Jan 2012)

Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism

  • Huijsdens-van Amsterdam Karin,
  • Barge-Schaapveld Daniela QCM,
  • Mathijssen Inge B,
  • Alders Mariëlle,
  • Pajkrt Eva,
  • Knegt Alida C

DOI
https://doi.org/10.1186/1755-8166-5-8
Journal volume & issue
Vol. 5, no. 1
p. 8

Abstract

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Abstract Double aneuploidy mosaicism of two different aneuploidy cell lines is rare. We describe for the first time a double trisomy mosaicism, involving chromosomes 7 and 13 in a fetus presenting with multiple congenital anomalies. No evidence for chimerism was found by DNA genotyping. The origin of both trisomies are consistent with isodisomy of maternal origin. Therefore, it is most likely that the double trisomy mosaicism arose from two independent events very early in embryonic development. The trisomy 7 and 13 cells were shown to be of maternal origin.

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