Atypical haemolytic uremic syndrome (aHUS) and membranoproliferative glomerulonephritis (MPGN), different diseases or a spectrum of complement-mediated glomerular diseases?

Historically, patients with kidney diseases caused by genetic or acquired dysregulation of the complement alternative pathway have been grouped into clinical syndromes, C3 glomerulopathy (C3GN/DDD) and thrombotic microangiopathy (TMA), specifically atypical haemolytic uremic syndrome (aHUS). Recent...

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Bibliografiska uppgifter
I publikationen:BMJ Case Rep
Huvudupphovsmän: Ankawi, Ghada A, Clark, William F
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Publishing Group 2017
Ämnen:
Rare Disease
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5624031/
https://ncbi.nlm.nih.gov/pubmed/28798244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2017-220974
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