RevieweNeurologicalSci2026
A comprehensive literature review of Wilson Disease in Africa.
Review in eNeurologicalSci, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Wilson Disease (WD) is an autosomal recessive disorder caused by mutations in the Methods: This narrative review synthesizes literature on WD epidemiology, diagnosis, and genetics in Africa, focusing on data from countries with published studies such as Morocco and Egypt. Information on clinical presentation, diagnostic criteria (Leipzig scoring, Kayser-Fleischer rings), and genetic profiles was compiled from peer-reviewed articles and case reports. Conclusion: WD is a significant but often overlooked genetic disorder in Africa, where diagnostic challenges and low awareness contribute to underreporting. Available data, primarily from Northern Africa, show a high frequency of consanguinity-related cases and distinct
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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.