ArticleCureus2025
Diagnostic Dilemmas of Wilson's Disease.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Microelements and biochemical biomarkers-based machine learning for predicting adverse pregnancy outcomes in Wilson's disease: risk stratification by integrating hepatic fibrosis and cerebral function.Frontiers in nutrition · 2026Article
- Multiscale computational genomics in Wilson disease: from atomic dynamics to clinical prediction.Frontiers in genetics · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Wilson's disease is a rare autosomal recessive disorder characterized by impaired hepatic copper transport, leading to copper accumulation in tissues and diverse clinical manifestations. A 27-year-old male chemical factory worker presented with acute haemolytic anaemia, pancytopenia, jaundice, and altered sensorium, indicative of acute liver failure. Despite normal serum ceruloplasmin levels, elevated 24-hour urinary copper levels (227.53 µg/24 hours) supported the diagnosis of probable Wilson's disease. The patient responded to symptomatic management, including transfusions and antibiotics, with gradual clinical and biochemical improvement before discharge against medical advice. This case underscores the diagnostic challenges of Wilson's disease due to nonspecific symptoms and limitations of laboratory tests. It highlights the importance of clinical suspicion and a multidisciplinary approach to ensure accurate diagnosis and timely treatment.
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What OpenQuestion holds
Registered trials
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.