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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Turk J Obstet Gynecol
Hauptverfasser: Avcıoğlu, Sümeyra Nergiz, Altınkaya, Sündüz Özlem, Küçük, Mert, Zafer, Emre, Demircan Sezer, Selda, Odabaşı, Ali Rıza
Format: Artigo
Sprache:Inglês
Veröffentlicht: Galenos Publishing 2015
Schlagworte:
Online Zugang: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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