Evidence map›Paper›PMID 35131845›Full record

ArticleClinical medicine & research2022

Pancreatic Insufficiency in a Child with p.Gly542* and c.2657+5G>A Heterozygote CFTR: A Case Report.

Fernanda Dos Anjos, Jonatha Wruck, Thiago Inácio Teixeira do Carmo, Victor Emanuel Miranda Soares, Débora Tavares de Resende E Silva, Margarete Dulce Bagatini, Sarah Franco Vieira de Oliveira Maciel

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical medicine & research, 2022. 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
0.2field-weighted citation impact, top 55% of its field
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, 1 citations in OpenAlex.

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

7 authors at 1 institution in 1 country.

Fernanda Dos AnjosMedicial student, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Jonatha WruckMedicial student, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Thiago Inácio Teixeira do CarmoMedicial student, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Victor Emanuel Miranda SoaresMedicial student, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Débora Tavares de Resende E SilvaPost-doctorate in immunology, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Margarete Dulce BagatiniBiological Sciences, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Sarah Franco Vieira de Oliveira MacielBiological Sciences, Federal University of Fronteira Sul, Chapecó, SC, Brazil sarahfvo@gmail.com.
Universidade Federal da Fronteira Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis is a monogenic and autosomal recessive disease. It is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator gene responsible for encoding the CFTR protein. Involvement of the gastrointestinal and respiratory systems is the main clinical manifestation. In this case, we report a heterozygous

Indexed as

Cystic FibrosisExocrine Pancreatic InsufficiencyCystic Fibrosis Transmembrane Conductance RegulatorGenotypeHeterozygoteHumansMutationCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulatorc.2657+5G>ACFTR heterozygousCystic FibrosisExocrine pancreatic insufficiencyp.Gly542*

Identifiers

PMID35131845
PMCPMC9390849
OpenAlexW4210876117

What Socratic holds

Textmetadata
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.