Evidence map›Paper›PMID 42346732›Full record

ArticleInternational journal of neonatal screening2026

Ethical and Clinical Boundaries in Genomics & Newborn Screening: A Brief Report from IPIC2025.

Raquel Yahyaoui, Lúcia Mamede, Martin Zach, James Taylor, Claire Booth, Rosalind Fisher, Věra Franková, Adli Ali, Johan Prevot, Martine Pergent and 2 more

Abstract readConference Proceedings
In one paragraph

Article in International journal of neonatal screening, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

12 authors.

Raquel YahyaouiLaboratory of Metabolic Disorders and Newborn Screening Center of Eastern Andalusia, Hospital Regional Universitario de Málaga, 29011 Malaga, Spain.ORCID 0000-0001-6789-1563
Lúcia MamedeInternational Patient Organisation for Primary Immunodeficiencies (IPOPI), 1050 Brussels, Belgium.ORCID 0000-0001-8206-8102
Martin ZachDepartment of Analytic Philosophy, Institute of Philosophy of the Czech Academy of Sciences, Jilská 1, 110 00 Prague, Czech Republic.ORCID 0000-0001-7181-0391
James TaylorSchool of Humanities and Social Sciences, The College of New Jersey, Ewing, NJ 08628, USA.
Claire BoothDepartment of Paediatric Immunology and Gene Therapy, Great Ormond Street Hospital for Children, NHS Foundation Trust, London WC1N 3JH, UK.
Rosalind FisherDepartment of Clinical Immunology, Oxford University Hospitals NHSFT, Oxford OX3 9DU, UK.ORCID 0009-0006-2715-1329
Věra FrankováInstitute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University, 121 08 Prague 2, Czech Republic.ORCID 0000-0002-1927-9596
Adli AliDepartment of Pediatric, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.ORCID 0000-0001-5615-5966
Johan PrevotInternational Patient Organisation for Primary Immunodeficiencies (IPOPI), 1050 Brussels, Belgium.
Martine PergentInternational Patient Organisation for Primary Immunodeficiencies (IPOPI), 1050 Brussels, Belgium.
Roberta Anido de PenaInternational Patient Organisation for Primary Immunodeficiencies (IPOPI), 1050 Brussels, Belgium.
Elizabeth RiversDepartment of Paediatric Immunology and Gene Therapy, Great Ormond Street Hospital for Children, NHS Foundation Trust, London WC1N 3JH, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Ethics Session of the International Primary Immunodeficiency Congress (IPIC), held in November 2025 and organised by the International Patient Organisation for Primary Immunodeficiencies (IPOPI), examined one of the most challenging developments emerging from genomic-enhanced newborn screening: the identification of serious, non-treatable disorders as incidental detection in programmes originally designed to detect severe combined immunodeficiency (SCID). Using a fictionalised clinical scenario based on the recent literature, the session explored the early diagnosis of ataxia-telangiectasia (AT) detected through TREC-based screening. The discussion highlighted the clinical value and psychological risks associated with presymptomatic detection, the persistent shortcomings in parental consent processes, the systemic pressures created by expanding genomic testing, and the ethical challenges surrounding the reporting and management of incidental findings in screening. The debate underscored the need for internationally coordinated frameworks to guide the management of incidental detection in newborn screening as genomic technologies become more deeply embedded in routine public health practice.

Indexed as

ataxia–telangiectasiaethicsgenomicsincidental detectionnewborn screening (NBS)population screeningsevere combined immunodeficiency (SCID)

Identifiers

PMID42346732
PMCPMC13299271

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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.