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

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), which is c...

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Detalles Bibliográficos
Autores principales: Alge, Joseph L., Wenderfer, Scott E., Hicks, John, Bekheirnia, Mir Reza, Schady, Deborah A., Kain, Jamey S., Braun, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516385/
https://www.ncbi.nlm.nih.gov/pubmed/28720077
http://dx.doi.org/10.1186/s12882-017-0643-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516385/
https://www.ncbi.nlm.nih.gov/pubmed/28720077
http://dx.doi.org/10.1186/s12882-017-0643-1

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