Evidence map›Paper›PMID 40213020›Full record

ArticleJCEM case reports2025

A Rare Cause of Acute Pancreatitis: Two Siblings With Werner Syndrome.

Kenan Sakar, Baris Akinci, Ilgin Yildirim Simsir, Tahir Atik, Gulhan Akbaba, Nese Cinar

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

Article in JCEM case reports, 2025. 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.

Kenan SakarDepartment of Endocrinology and Metabolism, Mugla Sitki Kocman University, Mugla 48000, Turkey.ORCID https://orcid.org/0000-0002-3254-7815
Baris AkinciIzmir International Biomedicine and Genome Institute, Dokuz Eylul University, Izmir 35340, Turkey.
Ilgin Yildirim SimsirDepartment of Endocrinology and Metabolism, Ege University, Izmir 35100, Turkey.
Tahir AtikDepartment of Child Genetic Diseases, Ege University, Izmir 35100, Turkey.ORCID https://orcid.org/0000-0002-1142-3872
Gulhan AkbabaDepartment of Endocrinology and Metabolism, Mugla Sitki Kocman University, Mugla 48000, Turkey.
Nese CinarDepartment of Endocrinology and Metabolism, Mugla Sitki Kocman University, Mugla 48000, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipodystrophies are rare disorders characterized by loss of body fat resulting in leptin deficiency. Patients are predisposed to metabolic complications such as severe insulin resistance, hypertriglyceridemia, and hepatic steatosis. Werner syndrome (WS) is among the progeroid syndromes in the classification of lipodystrophy. In this case report, we describe two siblings. In the first case, lipodystrophy was suspected when the patient presented with acute pancreatitis and hypertriglyceridemia, and a diagnosis of WS was confirmed. Subsequently, genetic screening of the patient's sister, who had early-onset diabetes, also revealed WS.

Indexed as

acute pancreatitishypertriglyceridemialipodystrophyWerner syndrome

Identifiers

PMID40213020
PMCPMC11982666

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.