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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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| Publicado no: | Turk J Obstet Gynecol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Galenos Publishing
2015
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| Assuntos: | |
| Acesso em linha: | 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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