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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
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dc.contributor.authorPatel, Priyal-
dc.contributor.authorKotecha, Dhruv-
dc.contributor.authorPandya, Hetal-
dc.date.accessioned2019-07-02T10:15:19Z-
dc.date.available2019-07-02T10:15:19Z-
dc.date.issued2018-03-
dc.identifier.issn2319-7064-
dc.identifier.urihttp://localhost:80/xmlui/handle/123456789/165-
dc.description.abstractWilson 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.en_US
dc.language.isoen_USen_US
dc.publisherInternational Journal of Science and Researchen_US
dc.subjectWilsons Diseaseen_US
dc.subjectHepatitis Een_US
dc.titleSilent Wilsons Disease Unmasked By Hepatitis E Case Studyen_US
dc.typeArticleen_US
Appears in Collections:Faculty Publications

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