Evidence map›Paper›PMID 41103600›Full record

ArticleClinical case reports2025

Persistent Ompahalomesenteric Duct in a Newborn With 16p11.2 Deletion: Report of New Findings.

Surasak Puvabanditsin, Sathyaprasad Burjonrappa, Natasha Cordero, Su Young Park, Jenny Choi, Amrryn Halari, Dawn Arumemi, Rajeev Mehta

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Surasak PuvabanditsinDepartment of Pediatrics Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.ORCID https://orcid.org/0000-0002-7467-5874
Sathyaprasad BurjonrappaDepartment of Surgery Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.
Natasha CorderoRutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.
Su Young ParkRutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.ORCID https://orcid.org/0009-0001-5995-9123
Jenny ChoiErnest Mario School of Pharmacy Rutgers University New Brunswick New Jersey USA.
Amrryn HalariRutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.ORCID https://orcid.org/0009-0004-6791-121X
Dawn ArumemiDepartment of Surgery Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.
Rajeev MehtaRutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA.ORCID https://orcid.org/0000-0003-3075-4498

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Omphalomesenteric duct (OMD) is an embryologic communication between the extraembryonic yolk sac and the primitive midgut. The OMD malformations are relatively rare diseases associated with developmental defects related to the closure of the omphalomesenteric duct. These malformations can present in various forms, including cysts, fistulas, or sinuses, and may be either asymptomatic or symptomatic. Meckel's diverticulum is the most common outcome of failed OMD resorption. We report a case of a newborn with a symptomatic OMD malformation associated with a 16p11.2 microdeletion. This is the first case report of this association, and we present a literature review.

Indexed as

16p11.2 microdeletioncongenital malformationintestinal obstructionomphalomesenteric ductumbilical anomaly

Identifiers

PMID41103600
PMCPMC12521818

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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.