Acute renal failure in a 7-year-old boy: do not miss rare and treatable cause
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-021-01190-z.pdf
Reference8 articles.
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3. Beck BB, van Spronsen F, Diepstra A, Berger RM, Kömhoff M (2017) Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity. Pediatr Nephrol 32:733–741
4. Guigonis V, Frémeaux-Bacchi V, Giraudier S, Favier R, Borderie D, Massy Z, Mougenot B, Rosenblatt DS, Deschênes G (2005) Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation. Am J Kidney Dis 45:588–595
5. Caillaud C, Zaloszyc A, Licht C, Pichault V, Fremeaux-Bacchi V, Fischbach M (2016) CFH gene mutation in a case of Shiga toxin associated hemolytic uremic syndrome (STEC-HUS). Pediatr Nephrol 31:157–161
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1. Concurrent Cobalamin C and Plasminogen Deficiencies in a Patient with Chronic Thrombotic Microangiopathy;Nephron;2023-08-23
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