Evidence map›Paper›PMID 42056489›Full record

ArticleEuropean radiology2026

Phenotyping trisomies 13 and 18 and CHARGE syndrome in fetal MRI-a proposed phenome-based, morphological disease severity score, and network medicine analysis.

Marlene Stuempflen, Michael Weber, Ursula Schwarz-Nemec, Anke Scharrer, Hui Shi, Victor U Schmidbauer, Patric Kienast, Katharina Goeral, Guelen Yerlikaya-Schatten, Gregor Kasprian and 1 more

Abstract read
In one paragraph

Article in European radiology, 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

11 authors.

Marlene StuempflenDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Michael WeberDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Ursula Schwarz-NemecDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Anke ScharrerDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Hui ShiDepartment of Radiology, Zhu Jiang Hospital, Southern Medical University, Guangzhou, China.
Victor U SchmidbauerDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Patric KienastDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Katharina GoeralDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Guelen Yerlikaya-SchattenDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Gregor KasprianDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Daniela PrayerDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria. daniela.prayer@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-4612-2356

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCHARGE syndrome (CS) and trisomy 13 (T13) and 18 (T18) are heterogeneous diseases with overlapping morphological features. Historically, T13 and T18 were deemed incompatible with life. Recently, numerous studies have reported prolonged survival for some affected patients. Consequently, the question of individual counseling has arisen. This study aimed to analyze the fetal MRI-based phenome of CS, T13, and T18. MATERIALS AND

methodsFetal MRI-based phenotyping was conducted, and a morphological disease severity score that assessed 16 anatomical regions was proposed. Furthermore, a co-occurrence analysis was generated to visualize the overlapping and differentiating features of CS, T13, and T18.

resultsForty-eight fetuses who underwent fifty-seven fetal MRI scans were analyzed. Disease severity scores ranged from 1-25 (mean 12.7) and highlighted heterogeneous disease manifestations among investigated patients. In the co-occurrence analysis the T13 network showed the highest complexity.

conclusionConsidering recent trends towards a change in management from mostly palliative to therapeutic care for patients with CS, T13, and T18, care providers face challenging decisions regarding management. The proposed preliminary MRI-based phenotyping score and the provided phenome visualization aim to aid physicians in counseling and choosing appropriate management plans. Future studies will be necessary to correlate prenatal imaging findings to outcome data in larger patient collectives. KEY POINTS: Question What are the phenotypical presentations of CHARGE syndrome, trisomy 13, and trisomy 18 in fetal MRI and can prenatal MRI findings help clinicians in predicting postnatal outcomes? Findings MRI phenomes were visualized in co-occurrence networks, and a preliminary disease severity score was proposed, based on available outcome data, to aid in risk stratification. Clinical relevance Recent trends in management, a shift from mostly palliative to therapeutic care for affected patients, have challenged clinicians. The provided phenome visualization of these heterogeneous diseases and the proposed disease severity score may aid physicians in counseling and selecting appropriate pregnancy management.

Indexed as

CHARGE SyndromeMagnetic Resonance ImagingPrenatal DiagnosisTrisomy 13 SyndromeTrisomy 18 SyndromeFemaleHumansPhenotypePregnancySeverity of Illness IndexCHARGE syndromeFetal MRIMagnetic resonance imagingTrisomy 13Trisomy 18

Identifiers

PMID42056489
PMCPMC13342138

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.