Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation and IgA Nephropathy: A Case Report Successfully Treated with Eculizumab-Reference-Cited by-同舟云学术

Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation and IgA Nephropathy: A Case Report Successfully Treated with Eculizumab

Published:2017-12-14 Issue:4 Volume:138 Page:324-327
ISSN:1660-8151
Container-title:Nephron
language:en
Short-container-title:Nephron

Author:

Nakamura Hironori,Anayama Mariko,Makino Mutsuki,Makino Yasushi,Tamura Katsuhiko,Nagasawa Masaki

Publisher

S. Karger AG

Reference18 articles.

1. Moake JL: Thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome. Arch Pathol Lab Med 2002; 126: 1430–1433.

2. Noris M, Remuzzi G: Atypical hemolytic-uremic syndrome. N Engl J Med 2009; 361: 1676–1687.

3. Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ: Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat 2010; 31:E1445–E160.

4. Manenti L, Gnappi E, Vaglio A, Allegri L, Noris M, Bresin E, Pilato FP, Valoti E, Pasquali S, Buzio C: Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature. Nephrol Dial Transplant 2013; 28: 2246–2259.

5. Wang R, Zhang Y, Li S, Chen H, Zeng C, Chen H, Tang Z, Liu Z: Hemolytic uremic syndrome complicated with IgA nephropathy: a case report and literature review. Clin Nephrol 2015; 83: 36–40.

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