Atypical hemolytic uremic syndrome
Definition:
References:
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[1]. David Kavanagh, et al. Atypical haemolytic uraemic syndrome. Br Med Bull. 2006;77-78:5-22. [Content Brief]
[2]. Elena Goicoechea de Jorge, et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A. 2007 Jan 2;104(1):240-5. [Content Brief]
[3]. Marina Noris, et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet. 2003 Nov 8;362(9395):1542-7. [Content Brief]
[4]. Mieke Delvaeye, et al. Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med. 2009 Jul 23;361(4):345-57. [Content Brief]
[5]. P Warwicker, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int. 1998 Apr;53(4):836-44. [Content Brief]
[6]. Peter F Zipfel, et al. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. PLoS Genet. 2007 Mar 16;3(3):e41. [Content Brief]
[7]. V Fremeaux-Bacchi, et al. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet. 2004 Jun;41(6):e84. [Content Brief]
[8]. Veronique Frémeaux-Bacchi, et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. Blood. 2008 Dec 15;112(13):4948-52. [Content Brief]
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