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Abstract
Objective: This study aims to highlight the importance of early recognition and diagnosis of Wilson’s disease (WD) in young adults presenting with chronic liver disease (CLD) of unknown etiology.
Design, Materials, and Methods: A single case study of a 30-year-old non-alcoholic male presenting with CLD and negative viral hepatitis markers. A comprehensive evaluation including serological tests, 24-hour urinary copper levels, and ceruloplasmin levels was conducted to confirm the diagnosis of WD.
Results: The patient exhibited hepatic manifestations without neurological symptoms. Despite a negative Kayser-Fleischer (KF) ring, elevated urinary copper excretion and reduced ceruloplasmin levels led to a confirmed diagnosis of WD. Early initiation of copper chelation therapy with penicillamine and zinc supplementation resulted in significant clinical and biochemical improvement over three months.
Conclusion: Wilson’s disease should be considered in young patients with unexplained CLD, even in the absence of neurological symptoms and KF rings. Prompt diagnosis and treatment can prevent disease progression and improve long-term outcomes.
"Case Report: Wilson’s Disease Presenting as Chronic Liver Disease in a Non-Alcoholic Adult Male", International Journal for Research Trends and Innovation (www.ijrti.org), ISSN:2455-2631, Vol.10, Issue 3, page no.a425-a427, March-2025, Available :http://www.ijrti.org/papers/IJRTI2503054.pdf
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ISSN:
2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator