Evidence map›Paper›PMID 41387180›Full record

ArticleJournal of clinical laboratory analysis2026

False Positive or False Negative-An Interesting Case in Prenatal Diagnostic Laboratory.

Pingping Zhang, Yanmei Sun, Haishen Tian, Xuedong Shi, Limin Rong, Yali Li

Abstract readCase Reports
In one paragraph

Article in Journal of clinical laboratory analysis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Pingping ZhangDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.
Yanmei SunDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.ORCID https://orcid.org/0000-0001-8862-0762
Haishen TianDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.
Xuedong ShiDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.
Limin RongDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.
Yali LiDepartment of Reproductive and Genetics, Hebei General Hospital, Shijiazhuang, Hebei, China.ORCID https://orcid.org/0000-0002-9494-8462

Funding

government-funded project on clinical medical talent training ZF2023191high level talents funding project of Hebei province C20231018medical technology tracking and application project of Hebei province GZ2024008science and technology support plan of Hebei province 22377792D
6 · The paper itself

Abstract

backgroundPrenatal diagnosis relies on diverse clinical laboratory techniques to assess the health status of a developing fetus in utero. When multiple diagnostic methods applied to the same fetal sample yield discordant results, some suggestive of abnormalities and others normal, this discrepancy poses substantial challenges to accurate clinical interpretation and decision-making. CASE PRESENTATION: A 23-year-old pregnant woman underwent non-invasive prenatal testing (NIPT) that yielded an abnormal fetal screening result. Subsequent prenatal diagnostic assessments, including single nucleotide polymorphism (SNP)-Array analysis and prenatal BACs-on-Beads (PNBoBs) assay, suggested a normal fetal karyotype. However, conventional karyotypic analysis and fluorescence in situ hybridization (FISH) uncovered fetal chromosomal abnormalities.

conclusionsDifferent diagnostic techniques possess distinct strengths, limitations, and applicable scopes. Certain abnormalities may evade detection by a single technique due to technical constraints or sample-specific biological characteristics. Therefore, in prenatal diagnosis, clinicians should select suitable diagnostic modalities based on clinical context. When necessary, multiple complementary methods should be employed for cross-validation to approximate the true fetal status and avoid missed diagnoses and misdiagnoses.

Indexed as

Prenatal DiagnosisChromosome AberrationsFalse Negative ReactionsFalse Positive ReactionsFemaleHumansIn Situ Hybridization, FluorescenceKaryotypingNoninvasive Prenatal TestingPolymorphism, Single NucleotidePregnancyYoung AdultBACs‐on‐Beadsfluorescence in situ hybridizationkaryotype analysisprenatal diagnosisSNP‐Array analysis

Identifiers

PMID41387180
PMCPMC12795981

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.