Evidence map›Paper›PMID 40978909›Full record

ArticleCureus2025

Morgagni Hernia in an Adolescent With Trisomy 21: An Uncommon Presentation in a Common Syndrome.

Chaimae N'joumi, Hasnae Elhaddadi, Lamiae Maazouz, Imane Skiker, Abdeladim Babakhouya, Maria Rkain

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2025. 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

6 authors.

Chaimae N'joumiDepartment of Pediatrics, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Hasnae ElhaddadiDepartment of Pediatrics, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Lamiae MaazouzDepartment of Radiology, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Imane SkikerDepartment of Radiology, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Abdeladim BabakhouyaDepartment of Pediatrics, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Maria RkainDepartment of Pediatrics, University Hospital Mohammed VI, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morgagni hernia (MH) is a rare type of congenital diaphragmatic hernia (CDH), representing 1-5% of cases, and it often presents with nonspecific or incidental findings. We report a case of a 15-year-old female with trisomy 21 who presented with abdominal distension and intermittent fever. Imaging studies, including chest radiograph and CT scan, revealed a right-sided MH containing omental and colonic structures. The patient underwent successful surgical repair. This report emphasizes the importance of considering congenital diaphragmatic anomalies in patients with genetic syndromes who present with atypical symptoms, and highlights the crucial role of thorough radiologic evaluation for accurate diagnosis and management.

Indexed as

diaghragmatic herniadown's syndromemorgagni’s herniaradiological diagnosistrisomy 21

Identifiers

PMID40978909
PMCPMC12450031

What OpenQuestion 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 OpenQuestion graph.