Evidence map›Paper›PMID 39588395›Full record

ArticleCureus2024

Retinitis Pigmentosa Associated With EYS Gene Mutations in Puerto Rico: A Case Series.

Armando J Ruiz-Justiz, Leonardo J Molina Thurin, Andres Emanuelli, Natalio Izquierdo

Abstract read
In one paragraph

Article in Cureus, 2024. 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

4 authors.

Armando J Ruiz-JustizDepartment of Ophthalmology, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.
Leonardo J Molina ThurinDepartment of Medicine, San Juan Bautista School of Medicine, Caguas, PRI.
Andres EmanuelliDepartment of Ophthalmology, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.
Natalio IzquierdoDepartment of Surgery, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutations in the

methodsThis retrospective case series was conducted at two major ophthalmology clinics in Puerto Rico from 2019 to 2023. A chart review was performed to identify RP patients who had mutations in the

resultsSeven Puerto Rican patients, three females (43%) and four males (57%), with a clinical diagnosis of RP, were found to have pathogenic

Indexed as

aberrant splicingautosomal recessive retinitis pigmentosaeyes genegenetic analysisrare genetic diseasestruncating mutations

Identifiers

PMID39588395
PMCPMC11588300

What OpenQuestion holds

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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.