Two cases of atypical hemolytic uremic syndrome (aHUS) and eosinophilic granulomatosis with polyangiitis (EGPA): a possible relationship

Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by hemolysis, thrombocytopenia, and renal failure. It is related to genetic mutations of the alternative complement pathway and is difficult to differentiate from other prothrombotic microangiopathies. Eosinophilic granulomato...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:CEN Case Rep
Main Authors: Cao, Mercedes, Ferreiro, Tamara, Leite, Bruna N., Pita, Francisco, Bolaños, Luis, Valdés, Francisco, Alonso, Angel, Vázquez, Eduardo, Mosquera, Juan, Trigás, María, Rodríguez, Santiago
Format: Artigo
Sprog:Inglês
Udgivet: Springer Japan 2017
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5438815/
https://ncbi.nlm.nih.gov/pubmed/28509134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-017-0251-8
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker