Evidence map›Paper›PMID 41626296›Full record

ArticleCase reports in pediatrics2026

PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report.

Rosita Saul, Maya David, Jordin Frasch, Pedro A Sanchez-Lara, Bahareh M Schweiger

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Rosita SaulDepartment of Osteopathic Medical Education, Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, Florida, USA, nova.edu.ORCID https://orcid.org/0009-0000-0913-3385
Maya DavidDivision of Pediatric Endocrinology, Guerin Children's, Cedars-Sinai Medical Center, Los Angeles, California, USA, cedars-sinai.edu.ORCID https://orcid.org/0009-0004-9206-5246
Jordin FraschDivision of Pediatric Endocrinology, Guerin Children's, Cedars-Sinai Medical Center, Los Angeles, California, USA, cedars-sinai.edu.ORCID https://orcid.org/0000-0003-1621-7688
Pedro A Sanchez-LaraDivision of Pediatric Genetics, Guerin Children's, Cedars-Sinai Medical Center, Los Angeles, California, USA, cedars-sinai.edu.
Bahareh M SchweigerDivision of Pediatric Endocrinology, Guerin Children's, Cedars-Sinai Medical Center, Los Angeles, California, USA, cedars-sinai.edu.ORCID https://orcid.org/0000-0002-3928-5221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report an 11-year-old Hispanic male with a PPP1R12A gene de novo heterozygous likely pathogenic mutation, p. (Gln13Arg) (CAG>CGG), c.38

Identifiers

PMID41626296
PMCPMC12852962

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.