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Wilson’s disease

Sheeja Sebastian, Jancy J

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Indian Journal of Surgical Nursing 12(1):p 21-23, January – April 2023. | DOI: https://doi.org/10.21088/ijsn.2277.467X.12123.3

How Cite This Article:

Jancy J, Sheeja Sebastian/Wilson’s disease/Indian J Surg Nurs. 2023;12(1):21–23.

Timeline

Received : October 08, 2022         Accepted : November 10, 2022          Published : April 30, 2023

Abstract

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.


References

  • 1.   Harrison’s. Principals of Internal Medicine. 16th edition, volume 1.
  • 2.   Nicki R. Colledge, Brain R. Walker, Stuart H. Ralston. Davidsons Principal and practice of Medicine. Elsevier publishers. 21st edition. Pp- 960-962.
  • 3.   Nagral et al., Wilson's Disease: Clinical Practice Guidelines of the Indian National Association for Study of the Liver, the Indian Society ofPediatric Gastroenterology, Hepatology and Nutrition, and the Movement Disorders Society of India, Journal of Clinical and Experimental Hepatology (2018), https://doi.org/10.1016/j.jceh.2018.08.009.
  • 4.   Larry E. Johnson, MDS Mannual professional version Wilson’s disease. https://www.msdmanuals.com/en-in/professional/nutritional-disorders/mineraldeficiency-and-toxicity/wilson-disease.
  • 5.   Prasad M,DavidD.Wilson disease: A case study.Indian J ContNsg Edn2016[2022 Oct8];17:57-61:http://www.ijcne.org/text.asp?2016/17/2/57/286300.

Data Sharing Statement

There are no additional data available. All raw data and code are available upon request.

Funding

This research received no funding.

Author Contributions

All authors contributed significantly to the work and approve its publication.

Ethics Declaration

This article does not involve any human or animal subjects, and therefore does not require ethics approval.

Acknowledgements

We would like to express our gratitude to the patients, their families, and all those who have contributed to this study.

Conflicts of Interest

No conflicts of interest in this work.


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Cite this article

Jancy J, Sheeja Sebastian/Wilson’s disease/Indian J Surg Nurs. 2023;12(1):21–23.


Licence:

Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

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

DOI: https://doi.org/10.21088/ijsn.2277.467X.12123.3

Keywords

CeruloplasmincopperWilson’s disease

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Received October 08, 2022
Accepted November 10, 2022
Published April 30, 2023

licence


Attribution-Non-commercial 4.0 International (CC BY-NC 4.0)

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.


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