Evidence map›Paper›PMID 32181025›Full record

ArticleCase reports in endocrinology2020

Recurrent Hypoglycemia in a Case of Congenital Analbuminemia.

Martin Litzel, Gianluca Caridi, Francesca Lugani, Monica Campagnoli, Lorenzo Minchiotti, Stefan Fischli

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

Article in Case reports in endocrinology, 2020. 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
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  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

6 authors at 3 institutions in 2 countries.

Martin LitzelDivision of Endocrinology, Diabetes and Clinical Nutrition, Luzerner Kantonsspital, Luzern 6000, Switzerland.
Gianluca CaridiLaboratory of Molecular Nephrology, Istituto Giannina Gaslini, IRCCS, Genoa 16147, Italy.ORCID https://orcid.org/0000-0001-6700-3001
Francesca LuganiLaboratory of Molecular Nephrology, Istituto Giannina Gaslini, IRCCS, Genoa 16147, Italy.ORCID https://orcid.org/0000-0002-4189-8561
Monica CampagnoliDepartment of Molecular Medicine, University of Pavia, Pavia 27100, Italy.ORCID https://orcid.org/0000-0002-0983-6854
Lorenzo MinchiottiDepartment of Molecular Medicine, University of Pavia, Pavia 27100, Italy.ORCID https://orcid.org/0000-0002-7043-482X
Stefan FischliDivision of Endocrinology, Diabetes and Clinical Nutrition, Luzerner Kantonsspital, Luzern 6000, Switzerland.ORCID https://orcid.org/0000-0003-1659-343X
Istituto Giannina Gaslini · ITLuzerner Kantonsspital · CHUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In congenital analbuminemia (CAA), mutations in the albumin gene result in a severe deficiency or absence of plasma albumin. Only about 90 cases have been reported to date, but the specific features of glucose and lipid metabolism in congenital analbuminemia have only been studied in a rat model of analbuminemia. We report the case of a female patient hospitalized for a streptococcal skin infection who showed recurrent hypoglycemia. A diagnosis of CAA was confirmed by mutation analysis and by the detection of a single base variation in the

Identifiers

PMID32181025
PMCPMC7063871
OpenAlexW3007149201

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.