Full Text (PDF)
Review Article

Wilson’s disease

Sheeja Sebastian, 2 Assistant Professor, Jubilee Mission College of Nursing, Thrissur, Kerala 680005, India. , Jancy J , Sheeja Sebastian

Author Information

Licence:



Indian Journal of Surgical Nursing 12(1):p 21-23, . | DOI: DOI: http://dx.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.


Received : N/A         Accepted : N/A          Published : N/A

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

No records found.


Funding


Author Information

Authors and Affiliatione

  • Sheeja Sebastian, 2 Assistant Professor, Jubilee Mission College of Nursing, Thrissur, Kerala 680005, India.
    ,
  • Jancy J
    ,
  • Sheeja Sebastian
    ,

Conflicts of Interest

Supplementary Information

Below is the link to the supplementary material.


Rights and Permissions



About this article


Cite this article

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


Licence:



Download citation

Received Accepted Published
N/A N/A N/A
DOI: DOI: http://dx.doi.org/10.21088/ijsn.2277.467X.12123.3
Keywords CeruloplasmincopperWilson’s disease

Article Level Metrics

Last Updated

Sunday 08 June 2025, 09:06:03 (IST)


3

Accesses

00
0
00

Citations


22
11
23

View full article metrics including social shares, article views and publishing history


Article Keywords


Keyword Highlighting

Highlight selected keywords in the article text.


Timeline


Received N/A
Accepted N/A
Published N/A

licence



Access this article




Share