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- W4224137972 abstract "Wilson’s disease is a rare inherited autosomal recessive disorder of copper metabolism leading to various clinical, biochemical and radiological features. In this disorder there is accumulation of copper in various tissues like liver, brain, cornea, etc., due to impairment in excretion of copper from body. In today’s world Wilson’s disease has been evolved from fatal disease to a treatable condition were life expectancy and quality of life has been increased to a great extent. With advancement in diagnostic modalities there has been a drastic change in understanding the disease pathology and to nd treatment for better outcome for the patients. Earlier when there were delay in diagnosis and treatment of these patients, it led to early fatalities but is uncommon now. We present you a case of a 20 year male patient who was diagnosed with Wilson disease after he developed liver cirrhosis which proved fatal for him." @default.
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- W4224137972 date "2022-03-01" @default.
- W4224137972 modified "2023-09-23" @default.
- W4224137972 title "WILSON’S DISEASE A RARE AND FATAL DISEASE: CASE REPORT AND REVIEW OF LITERATURE" @default.
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- W4224137972 doi "https://doi.org/10.36106/ijsr/2704064" @default.
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