Evidence map›Paper›PMID 36304180›Full record

ArticleCase reports in endocrinology2022

A Case Report about Glycogenic Hepatopathy.

L Plaza Enriquez, N Konindala, H Yeh, P Khatiwada, M Sanchez Valenzuela, K Askari

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Persistent Lactatemia in Mauriac Syndrome.Case reports in endocrinology · 2024
    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 2 institutions in 1 country.

L Plaza EnriquezInternal Medicine Residency, Memorial Healthcare System, Hollywood, FL, USA.ORCID https://orcid.org/0000-0002-2553-8769
N KonindalaInternal Medicine Residency, Memorial Healthcare System, Hollywood, FL, USA.
H YehInternal Medicine Residency, Memorial Healthcare System, Hollywood, FL, USA.
P KhatiwadaInternal Medicine Residency, Memorial Healthcare System, Hollywood, FL, USA.
M Sanchez ValenzuelaInternal Medicine Residency, St. Barnabas Hospital, Bronx, NY, USA.
K AskariDepartment of Endocrinology Memorial Healthcare System, Hollywood, FL, USA.
Memorial Healthcare System · USSt. Barnabas Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Glycogenic hepatopathy is a rare complication of uncontrolled diabetes mellitus that presents with hepatomegaly and transient elevation in serum aminotransferase enzymes. The underlying pathophysiology involves excessive accumulation of intrahepatic glycogen. Glycogenic hepatopathy is usually underdiagnosed because it is difficult to differentiate from other entities, such as the nonalcoholic fatty liver. The gold standard for diagnosis is liver biopsy. Glycogenic hepatopathy can be reversed by the achievement of adequate glycemic control. Conclusion: Glycogenic hepatopathy must be suspected in patients with uncontrolled type 1 diabetes mellitus who present with elevated liver enzymes and hepatomegaly. Treating this rare condition requires a timely diagnosis with liver biopsy and strict glycemic control.

Identifiers

PMID36304180
PMCPMC9596235
OpenAlexW4306722548

What OpenQuestion holds

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LicenceCC BY
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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.