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Introduction Wilsons disease is a genetic disorder characterised by abnormal copper metabolism, leading to excessive copper deposition , primarily in the liver and brain. The condition typically has a juvenile onset (before 16 years of age), though it can present at any stage of life

[DOI] [PMC free article] [PubMed] [Google Scholar] 174.Breiteneder H., Peng Y.Q., Agache I., Diamant Z., Eiwegger T., Fokkens W.J., Traidl-Hoffmann C., Nadeau K., OHehir R.E., OMahony L

What are the leading causes of hyperpigmentation