Complement factor H mutation associated with membranoproliferative glomerulonephritis with transformation to atypical haemolytic uraemic syndrome

A patient with a history of haemolytic anaemia and membranoproliferative glomerulonephritis type 1 since childhood developed relapsing atypical haemolytic uraemic syndrome (aHUS) at the age of 18. Despite several episodes of relapsing aHUS, she was successfully treated with plasmapheresis. aHUS is s...

Full description

Saved in:
Bibliographic Details
Main Authors: Janssen van Doorn, Karin, Dirinck, Eveline, Verpooten, Gert A., Couttenye, Marie M.
Format: Artigo
Language:Inglês
Published: Oxford University Press 2013
Subjects:
Clinical Cases
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4086369/
https://ncbi.nlm.nih.gov/pubmed/25006455
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfs190
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items