ArticleInternational journal of legal medicine2025
Discovery and comprehensive analysis of a congenital chimerism via paternity testing using short tandem repeat genotyping.
Article in International journal of legal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In medical forensics, the detection of more than two alleles at a single locus is generally interpreted as a mixed sample or contamination. However, this can also indicate chimerism, in which an individual contains two or more distinct cell lines with different genomes. Multiple alleles at a single locus can be identified using short tandem repeat (STR) genotyping. In this study, we report a case of chimerism in a child, in which multiple alleles were detected at several loci during routine paternity testing. In particular, two alleles were detected at six loci with markedly uneven peaks, and three alleles were detected at 10 loci using different analysis kits. Analysis of additional samples from the father, mother, and child revealed that the three alleles were only present in the child's blood. Comprehensive analyses of multiple data sets confirmed that the child had congenital chimerism. The findings of this study highlight the importance of conducting comprehensive evaluations of potential chimerism when multiple alleles are detected at a gene locus to ensure the accuracy and reliability of the results and improve the credibility of genetic evidence. After excluding other factors, the potential for chimerism should be acknowledged in legal practice to ensure accurate and reliable identification. Chimerism can be a major confounding factor, and unless professionals are aware of this condition, they may draw incorrect conclusions with serious ramifications for the individuals involved.
Indexed as
Identifiers
40338295What OpenQuestion holds
Registered trials
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.