Evidence map›Paper›PMID 41746483›Full record

ArticleThe international journal of cardiovascular imaging2026

Uhl's anomaly after Glenn shunt - clinical image of a rare congenital heart defect.

Kacper Jaros, Maja Butrym, Jarosław Rycaj, Mateusz Knop, Roland Fiszer

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In one paragraph

Article in The international journal of cardiovascular imaging, 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

5 authors.

Kacper JarosStudent Scientific Association at the Department of Pediatric Cardiology and Congenital Heart Defects, Silesian Center for Heart Diseases in Zabrze, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.ORCID http://orcid.org/0009-0005-4502-8706
Maja ButrymStudent Scientific Association at the Department of Pediatric Cardiology and Congenital Heart Defects, Silesian Center for Heart Diseases in Zabrze, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland. butrym.maja@gmail.com.ORCID http://orcid.org/0009-0003-5387-2881
Jarosław RycajDepartment of Cardiac Surgery, Transplantology, Vascular and Endovascular Surgery, Silesian Center for Heart Diseases in Zabrze, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.
Mateusz KnopDepartment of Pediatric Cardiology and Congenital Heart Defects, Silesian Center for Heart Diseases in Zabrze; Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.ORCID http://orcid.org/0000-0002-6834-3718
Roland FiszerDepartment of Pediatric Cardiology and Congenital Heart Defects, Silesian Center for Heart Diseases in Zabrze; Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.ORCID http://orcid.org/0000-0002-4555-0589

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uhl's anomaly is an extremely rare congenital heart defect, with approximately 100 cases reported since its first description in 1952 by Dr Henry Uhl. Characterized by partial or complete absence of the right ventricular myocardium, it leads to progressive right ventricle dilation and right heart failure. Due to its rarity, there is no consensus regarding its surgical or medical management. We present a case of an 18-year-old male patient with Uhl's anomaly diagnosed in early infancy, managed by palliative Glenn shunt. This report provides insight into management of this rare condition.

Indexed as

Fontan ProcedureHeart Defects, CongenitalHeart VentriclesAdolescentCardiomyopathy, DilatedHumansMalePalliative CareTreatment OutcomeVentricular Function, RightGlenn shuntHeart defects, CongenitalMagnetic resonance imaging, CardiovascularUhl’s anomalyVentricular dysfunction, Right

Identifiers

PMID41746483

What OpenQuestion holds

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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 OpenQuestion graph.