Evidence map›Paper›PMID 41766828›Full record

ArticleJNMA; journal of the Nepal Medical Association2025

Wilson's Disease with Lymphoproliferative Disorder: A Case Report.

Ashish Jha, Saroj Kumar Shah, Ravi Ranjan Pradhan

Abstract readCase Reports
In one paragraph

Article in JNMA; journal of the Nepal Medical Association, 2025. 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

3 authors.

Ashish JhaDepartment of Pediatrics, Madhesh Institute of Health Sciences, Janakpurdham, Dhanusha, Nepal.
Saroj Kumar ShahDepartment of Pediatrics, Kanti Childrens' Hospital, Maharajgunj, Kathmandu, Nepal.
Ravi Ranjan PradhanBeni Hospital, Beni, Myagdi, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson's disease is characterized by copper accumulation in organs like liver, brain, and eyes, presenting with a varied clinical features, making it challenging to diagnose. This report describes a case of Wilson's disease with unusual hematological features. A 12-year-old from Himalayan region presented with weakness, dysarthria, tremors. Initial investigations revealed pancytopenia, and bone marrow showed a lymphoproliferative disorder. He developed behavioral changes, a flat affect, and scanning speech. Wilson's disease was confirmed through Kayser-Fleischer rings, reduced serum ceruloplasmin levels, and elevated urinary copper, supported by imaging.

Indexed as

Hepatolenticular DegenerationLymphoproliferative DisordersCeruloplasminChildCopperDysarthriaHumansMalePancytopeniaCeruloplasminCopperhematological disorderneurological manifestationWilson's disease

Identifiers

PMID41766828
PMCPMC12831825

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.