Evidence map›Paper›PMID 36514475›Full record

ArticleClinical case reports2022

Congenital hyperinsulinism-A case of mild hypoglycemia in an adult, detected by family testing.

Felicia Baleanu, Georgiana Taujan, Mihaela Rosu, Olga Kosmopoulou, Blerta Ioanna Papadopoulou, Emese Boros, Laura Iconaru

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2022. 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

7 authors.

Felicia BaleanuDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.ORCID https://orcid.org/0000-0002-2774-8874
Georgiana TaujanDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.ORCID https://orcid.org/0000-0002-2946-4162
Mihaela RosuDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.
Olga KosmopoulouDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.
Blerta Ioanna PapadopoulouDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.
Emese BorosPaediatric Endocrinology Unit Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles Brussels Belgium.
Laura IconaruDepartment of Endocrinology, CHU Brugmann Université Libre de Bruxelles Brussels Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup.

Indexed as

diabetesgenetic hyperinsulinismhypoglycemia

Identifiers

PMID36514475
PMCPMC9731303

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.