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Wilson’s disease presenting with HELLP syndrome; A case report
Wilson’s disease (WD) is an autosomal recessive disorder. It is characterized by toxic accumulation of copper mainly in the liver and brain but also in cornea and kidney due to a defect in biliary excretion of copper. The hepatic manifestation of WD is diverse and may include asymptomatic elevation...
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| Udgivet i: | Turk J Obstet Gynecol |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Galenos Publishing
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5558407/ https://ncbi.nlm.nih.gov/pubmed/28913043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjod.24434 |
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