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...

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Detalles Bibliográficos
Autores principales: Janssen van Doorn, Karin, Dirinck, Eveline, Verpooten, Gert A., Couttenye, Marie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Clinical Cases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086369/
https://www.ncbi.nlm.nih.gov/pubmed/25006455
http://dx.doi.org/10.1093/ckj/sfs190

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086369/
https://www.ncbi.nlm.nih.gov/pubmed/25006455
http://dx.doi.org/10.1093/ckj/sfs190

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