Evidence map›Paper›PMID 42088534›Full record

ArticleCase reports in women's health2026

False negativity for trisomy 18 in non-invasive prenatal testing: A case report.

Natália Andová, Vanda Repiská, Petra Priščáková, Lajos Gergely, Michaela Hýblová, Gabriel Minárik

Abstract readCase Reports
In one paragraph

Article in Case reports in women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Natália AndováInstitute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University Bratislava, Bratislava, Slovakia.
Vanda RepiskáInstitute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University Bratislava, Bratislava, Slovakia.
Petra PriščákováInstitute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University Bratislava, Bratislava, Slovakia.
Lajos GergelyInstitute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University Bratislava, Bratislava, Slovakia.
Michaela HýblováMEDIREX GROUP ACADEMY n.p.o., Nitra, Slovakia.
Gabriel MinárikTrisomy test Ltd., Nitra, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

False-negative results in non-invasive prenatal testing are rare but clinically significant, particularly in the presence of biological factors such as feto-placental mosaicism. This report describes a pregnancy affected by fetal trisomy 18 in which three consecutive non-invasive prenatal tests reported low risk despite abnormal first-trimester ultrasound findings (increased nuchal translucency, hydrops fetalis, and tricuspid regurgitation). Amniocentesis subsequently confirmed trisomy 18 in the fetus. Post-termination placental analysis revealed mosaicism, with high trisomy 18 levels on the fetal side (up to 76%) and lower levels on the maternal side (20%) of the placenta. This distribution resulted in an estimated "effective fetal fraction" below the standard detection threshold for a non-invasive prenatal test (∼4%). These findings highlight the limitations of non-invasive prenatal testing as a screening test and underscore the importance of invasive diagnostic testing when structural abnormalities are detected. Consideration of biological variables such as placental mosaicism is essential for accurate interpretation and clinical decision-making.

Indexed as

Diagnostic errorsMosaicismNon-invasive prenatal testingTrisomy 18 syndrome

Identifiers

PMID42088534
PMCPMC13137892

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