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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:CEN Case Rep
मुख्य लेखकों: Cao, Mercedes, Ferreiro, Tamara, Leite, Bruna N., Pita, Francisco, Bolaños, Luis, Valdés, Francisco, Alonso, Angel, Vázquez, Eduardo, Mosquera, Juan, Trigás, María, Rodríguez, Santiago
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Springer Japan 2017
विषय:
Case Report
ऑनलाइन पहुंच: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
टैग : टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!

समान संसाधन