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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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Detalhes bibliográficos
Publicado no:Turk J Obstet Gynecol
Main Authors: Avcıoğlu, Sümeyra Nergiz, Altınkaya, Sündüz Özlem, Küçük, Mert, Zafer, Emre, Demircan Sezer, Selda, Odabaşı, Ali Rıza
Formato: Artigo
Idioma:Inglês
Publicado em: Galenos Publishing 2015
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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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