Evidence map›Paper›PMID 39958070›Full record

ArticleCureus2025

Expanding the Gastrointestinal Phenotype of 10p15.3 Microdeletion Syndrome: Refractory Atypical Gastroparesis in an Adult.

Jeffrey Li, Vismaya Bachu, Bita Shahrvini, Mark Baniqued, Shida Haghighat, Niharika R Mallepally

Abstract readCase Reports
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.

Jeffrey LiInternal Medicine, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Vismaya BachuInternal Medicine, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Bita ShahrviniInternal Medicine, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Mark BaniquedInternal Medicine, Olive View University of California Los Angeles Medical Center, Los Angeles, USA.
Shida HaghighatVatche and Tamar Manoukian Division of Digestive Diseases, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.
Niharika R MallepallyVatche and Tamar Manoukian Division of Digestive Diseases, University of California Los Angeles David Geffen School of Medicine, Los Angeles, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

10p15.3 microdeletion syndrome is a rare genetic disorder characterized by the loss of

Indexed as

10p15.3 microdeletion syndromeatypical gastroparesisdip2c geneenteric nervous system dysfunctiongastroesophageal reflux disease (gerd)gastrointestinal motility disordersprucalopriderare genetic disordersrefractory gastrointestinal diseasezmynd11 gene

Identifiers

PMID39958070
PMCPMC11829799

What OpenQuestion holds

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LicenceCC BY
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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.