Evidence map›Paper›PMID 39728742›Full record

ArticlePediatric reports2024

Francesco Comisi, Consolata Soddu, Francesco Lai, Monica Marica, Michela Lorrai, Giancarlo Mancuso, Sabrina Giglio, Salvatore Savasta

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Pediatric reports, 2024. 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. Review
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.

Francesco ComisiPediatrics Department, Microcitemico Hospital "A. Cao", University of Cagliari, 09124 Cagliari, Italy.ORCID 0009-0002-8525-3041
Consolata SodduPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", ASL 8 Cagliari, 09121 Cagliari, Italy.
Francesco LaiPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", ASL 8 Cagliari, 09121 Cagliari, Italy.
Monica MaricaPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", ASL 8 Cagliari, 09121 Cagliari, Italy.
Michela LorraiMedical Genetics Unit, Department of Medical Sciences and Public Health, University of Cagliari, 09124 Cagliari, Italy.ORCID 0009-0002-6660-1784
Giancarlo MancusoMedical Genetics Unit, Department of Medical Sciences and Public Health, University of Cagliari, 09124 Cagliari, Italy.ORCID 0009-0004-4969-1321
Sabrina GiglioMedical Genetics Unit, Department of Medical Sciences and Public Health, University of Cagliari, 09124 Cagliari, Italy.ORCID 0000-0002-3954-326X
Salvatore SavastaPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", Department of Medical Sciences and Public Health, University of Cagliari, 09124 Cagliari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHouge-Janssens syndrome 1 is a condition with onset in early childhood caused by heterozygous pathogenic variants in the CASE PRESENTATION: We report the first

conclusionsHaemangiomas have never been linked to the syndromic phenotype of the

Indexed as

haemangiomasJordan’s syndromePI3K/AKT signalling pathwayPPP2R5D

Identifiers

PMID39728742
PMCPMC11677636

What Socratic 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 Socratic graph.