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Wilson's Disease is an autosomal-recessive disorder caused by mutation in the ATP7B gene which impairs copper excretion from the bile. Impaired copper transport and decrease copper secretion into bile which leads copper accumulation, first in the liver but ultimately in the brain and other tissues, produces clinical manifestations that may include hepatic, neurological, psychiatric and ophthalmological. Treatment is only palliative and intended to restore and maintain copper balance.
Jancy J, Sheeja Sebastian/Wilson’s disease/Indian J Surg Nurs. 2023;12(1):21–23.
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
| Received | Accepted | Published |
|---|---|---|
| October 08, 2022 | November 10, 2022 | April 30, 2023 |
Friday 24 July 2026, 06:43:09 (IST)
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| Received | October 08, 2022 |
| Accepted | November 10, 2022 |
| Published | April 30, 2023 |
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.