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DC Field | Value | Language |
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dc.contributor.author | Patel, Priyal | - |
dc.contributor.author | Kotecha, Dhruv | - |
dc.contributor.author | Pandya, Hetal | - |
dc.date.accessioned | 2019-07-02T10:15:19Z | - |
dc.date.available | 2019-07-02T10:15:19Z | - |
dc.date.issued | 2018-03 | - |
dc.identifier.issn | 2319-7064 | - |
dc.identifier.uri | http://localhost:80/xmlui/handle/123456789/165 | - |
dc.description.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. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | International Journal of Science and Research | en_US |
dc.subject | Wilsons Disease | en_US |
dc.subject | Hepatitis E | en_US |
dc.title | Silent Wilsons Disease Unmasked By Hepatitis E Case Study | en_US |
dc.type | Article | en_US |
Appears in Collections: | Faculty Publications |
Files in This Item:
File | Description | Size | Format | |
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ART20179760.pdf | 172.47 kB | Adobe PDF | ![]() View/Open |
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