Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report

Abstract Background Hemolytic uremic syndrome (HUS) can occur as a primary process due to mutations in complement genes or secondary to another underlying disease. HUS sometimes occurs in the setting of glomerular diseases, and it has been described in association with Denys-Drash syndrome (DDS), wh...

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Bibliographic Details
Main Authors: Joseph L. Alge, Scott E. Wenderfer, John Hicks, Mir Reza Bekheirnia, Deborah A. Schady, Jamey S. Kain, Michael C. Braun
Format: Article
Language:English
Published: BMC 2017-07-01
Series:BMC Nephrology
Subjects:
HUS
WT1
Online Access:http://link.springer.com/article/10.1186/s12882-017-0643-1