Evidence map›Paper›PMID 41111688›Full record

ArticleCureus2025

Genotype-Phenotype Correlation and Psychiatric Manifestations in a Case of Phelan-McDermid Syndrome With 22q13.33 Deletion.

Mario Alberto Puente Torres, Juan Jorge Palacios Casados, Yvonne Flores Medina, Aideé Gonzalez Gutierrez, Carlos Sabás Cruz Fuentes

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

5 authors.

Mario Alberto Puente TorresDepartment of Psychiatric Genetics, Ramón de la Fuente Muñiz National Institute of Psychiatry, Mexico City, MEX.
Juan Jorge Palacios CasadosDepartment of Psychiatric Genetics, Ramón de la Fuente Muñiz National Institute of Psychiatry, Mexico City, MEX.
Yvonne Flores MedinaDepartment of Clinical Research, Ramón de la Fuente Muñiz National Institute of Psychiatry, Mexico City, MEX.
Aideé Gonzalez GutierrezDepartment of Clinical Neuropsychology, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Tlalnepantla, MEX.
Carlos Sabás Cruz FuentesDepartment of Psychiatric Genetics, Ramón de la Fuente Muñiz National Institute of Psychiatry, Mexico City, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phelan-McDermid syndrome (PMS) (OMIM: 606232) is a rare genetic disorder usually caused by deletions in the 22q13.3 region, often affecting the

Indexed as

22q13.33 deletionbipolar disordercognitive-behavioral aspectsgenomic medicineintellectual disabilityneuropsychiatric symptomspersonalized medicinephelan-mcdermid syndromering chromosome 22shank3 gene

Identifiers

PMID41111688
PMCPMC12529893

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.