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Discordant NIPT result in a viable trisomy-21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy-14 cotwin.
Hochstenbach, Ron; Elferink, Martin G; van Zon, Patrick H A; Lichtenbelt, Klaske D; van Harssel, Jeske; Schuring-Blom, Heleen; Page-Christiaens, Godelieve C M L.
Afiliación
  • Hochstenbach R; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • Elferink MG; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • van Zon PHA; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • Lichtenbelt KD; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • van Harssel J; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • Schuring-Blom H; Department of Genetics University Medical Centre Utrecht Utrecht The Netherlands.
  • Page-Christiaens GCML; Department of Obstetrics and Gynecology University Medical Centre Utrecht Utrecht The Netherlands.
Clin Case Rep ; 6(5): 788-791, 2018 May.
Article en En | MEDLINE | ID: mdl-29744057
ABSTRACT
One of the confounders in noninvasive prenatal testing (NIPT) is the vanishing twin phenomenon. Prolonged contribution to the maternal Cell-free DNA (cfDNA) pool by cytotrophoblasts representing a demised, aneuploid cotwin may lead to a false-positive outcome for a normal, viable twin. We show that a vanishing trisomy-14 twin contributes to cfDNA for more than 2 weeks after demise.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2018 Tipo del documento: Article