Evidence map›Paper›PMID 42668699›Full record

ReviewCaspian journal of internal medicine2026

Diagnostic challenges and mimicking disorders of Wilson's Disease: A comprehensive review.

Seyyed-Saleh Hashemi, Aida Gholoobi, Karim Naghipoor, Tayebeh Hamzehloei

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Caspian journal of internal medicine, 2026. 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
–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

0 citing papers in PubMed.

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

4 authors.

Seyyed-Saleh HashemiMedical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Aida GholoobiMedical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Karim NaghipoorMedical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Tayebeh HamzehloeiMedical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson disease is classically defined as an autosomal recessive disorder of copper metabolism that leads to neurological and hepatic dysfunction. It is one of the most prevalent genetic liver disorders caused by pathogenic mutations in the

Indexed as

ATP7BCopper metabolismDifferential diagnosisWilson Disease (WD)

Identifiers

PMID42668699
PMCPMC13525243

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.