Wilson's disease
Main Article Content
Abstract
Wilson's disease is an autosomal recessive abnoramlaity in the hepatic excretion of copper that results in toxic accumulations of the metal in liver, brain and other organs. The disease occurs in populations of every ethnic and geographical origin and has a word wide prevalence of about I in 30,000 with a carrier frequency of I in abnormal gene (the locus on the long arm of chromosome 13) is present in all racial group studied so far and a higher incidence has been noted in Arabs. Chinese, Japanese and indians.
Article Details
How to Cite
1.
Saeedi I, Rehman S, Ilyas N. Wilson’s disease. J Postgrad Med Inst [Internet]. 2011 Sep. 22 [cited 2024 Oct. 3];16(2). Available from: https://www.jpmi.org.pk/index.php/jpmi/article/view/789
Issue
Section
Case Report
Work published in JPMI is licensed under a
Creative Commons Attribution-NonCommercial 2.0 Generic License.
Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.