Neonatal thrombotic microangiopathy secondary to factor I variant with Hirschsprung disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-020-00766-5.pdf
Reference19 articles.
1. Fakhouri F, Zuber J, Frémeaux-Bacchi V, Loirat C (2017) Haemolytic uraemic syndrome. Lancet 390(10095):681–696. https://doi.org/10.1016/S0140-6736(17)30062-4
2. Goodship TH, Cook HT, Fakhouri F, Fervenza FC, Frémeaux-Bacchi V, Kavanagh D et al (2017) Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int 91(3):539–551. https://doi.org/10.1016/j.kint.2016.10.005
3. Aigner C, Schmidt A, Gaggl M, Sunder-Plassmann G (2019) An updated classification of thrombotic microangiopathies and treatment of complement gene variant-mediated thrombotic microangiopathy. Clin Kidney J. 12(3):333–337. https://doi.org/10.1093/ckj/sfz040
4. Loirat C, Fakhouri F, Ariceta G, Besbas N, Bitzan M, Bjerre A et al (2016) An international consensus approach to the management of atypical hemolytic uremic syndrome in children. Pediatr Nephrol 31(1):15–39. https://doi.org/10.1007/s00467-015-3076-8
5. Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F et al (2007) A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation. Mol Immunol 44(8):1835–1844. https://doi.org/10.1016/j.molimm.2006.10.005
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