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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Detalles Bibliográficos
Autores principales: Avcıoğlu, Sümeyra Nergiz, Altınkaya, Sündüz Özlem, Küçük, Mert, Zafer, Emre, Demircan Sezer, Selda, Odabaşı, Ali Rıza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558407/
https://www.ncbi.nlm.nih.gov/pubmed/28913043
http://dx.doi.org/10.4274/tjod.24434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558407/
https://www.ncbi.nlm.nih.gov/pubmed/28913043
http://dx.doi.org/10.4274/tjod.24434

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