Home|Journals|Articles by Year|Audio Abstracts RSS - TOC
 

Case Report



Postpartum Diagnosed Wilson’s Disease

Serpil Aydogmus, Serenat Eris, Secil Kurtulmus, Huseyin Aydogmus, Emre Ekmekci, Fatih Demir, Sefa Kelekci.




Abstract

Wilson’s disease is an autosomal recessive genetic disorder in which defective biliary excretion of copper leads to its accumulation, especially in liver, brain and cornea. Clinical manifestations can vary widely. Untreated Wilson’s disease may lead to subfertility and pregnancy complications such as; recurrent miscarriages, induced hypertension, preeclampsia, placental abruption and intrauterine growth restriction. Here we present a case with Wilson’s disease (WD) diagnosed postpartum, underwent urgent cesarean section with a presumptive diagnosis of HELLP (Hemolysis, Elevated Liver Enzymes, Low Platelet Count) syndrome. Acute intravascular hemolytic anemia and thrombocytopenia in WD can be interpreted as a feature of HELLP syndrome besides acute liver failure. It should be considered in the diferrantial diagnosis.

Key words: Wilson’s disease, pregnancy, HELLP syndrome, postpartum, diferrantial diagnosis






Full-text options


Share this Article



Online Article Submission
• ejmanager.com
• ojshosting.net




eJManager.com
Review(er)s Central
JournalList
About BiblioMed
License Information
Terms & Conditions
Privacy Policy
Contact Us

The articles in Bibliomed are open access articles licensed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (https://creativecommons.org/licenses/by-nc-sa/4.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.