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Please use this identifier to cite or link to this item: http://172.20.40.131:8080/jspui/handle/123456789/165
Title: Silent Wilsons Disease Unmasked By Hepatitis E Case Study
Authors: Patel, Priyal
Kotecha, Dhruv
Pandya, Hetal
Keywords: Wilsons Disease
Hepatitis E
Issue Date: Mar-2018
Publisher: International Journal of Science and Research
Abstract: Wilson disease is a rare autosomal recessive inherited disorder of copper metabolism that is characterized by excessive deposition of copper in the liver, brain, and other tissues. Hepatitis E is a viral hepatitis caused by infection with a virus called hepatitis E virus. It is one of five known human hepatitis viruses. Although hepatitis E often causes an acute and self-limiting infection with low mortality rates in the western world, it bears a high risk of developing chronic hepatitis in immune compromised patients with substantial mortality rates. Reveal of Wilson’s disease with viral hepatitis is reported earlier in the literature as a rare association. Here we report a case of report 24 year old female patient with biochemical, serological, hematological and histopathological evidence of underlying Wilson’s disease complicated by hepatitis E virus infection. In this case the patient developed acute hepatic decompensation indicating that HEV plays a part in the acute hepatic decompensation seen in cases of unrecognized Wilson’s disease.
URI: http://localhost:80/xmlui/handle/123456789/165
ISSN: 2319-7064
Appears in Collections:Faculty Publications

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