Evidence map›Paper›PMID 26793401›Full record

ArticleCase reports in pediatrics2015

Clinical Phenotype of DiGeorge Syndrome with Negative Genetic Tests: A Case of DiGeorge-Like Syndrome?

Gianluigi Laccetta, Benedetta Toschi, Antonella Fogli, Veronica Bertini, Angelo Valetto, Rita Consolini

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in pediatrics, 2015. 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. 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

6 authors.

Gianluigi LaccettaPediatric Department, Faculty of Medicine, Rheumatology and Clinical Immunology Unit, Pisa University, 56126 Pisa, Italy.
Benedetta ToschiMedical Genetics Unit, Children Department, Pisa University, 56126 Pisa, Italy.
Antonella FogliCytogenetics and Molecular Genetics Unit, Children Department, Pisa University, 56126 Pisa, Italy.
Veronica BertiniCytogenetics and Molecular Genetics Unit, Children Department, Pisa University, 56126 Pisa, Italy.
Angelo ValettoCytogenetics and Molecular Genetics Unit, Children Department, Pisa University, 56126 Pisa, Italy.
Rita ConsoliniPediatric Department, Faculty of Medicine, Rheumatology and Clinical Immunology Unit, Pisa University, 56126 Pisa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a case of DiGeorge-like syndrome in which immunodeficiency coexisting with juvenile idiopathic arthritis, congenital heart disease, delay in emergence of language and in motor milestones, feeding and growing problems, enamel hypoplasia, mild skeletal anomalies, and facial dysmorphisms are associated with no abnormalities found on genetic tests.

Identifiers

PMID26793401
PMCPMC4697090

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.