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Case Reports
. 2022 Jul;35(6):1731-1735.
doi: 10.1007/s40620-021-01190-z. Epub 2021 Nov 13.

Acute renal failure in a 7-year-old boy: do not miss rare and treatable cause

A Boussetta  1   2   3   4   5 , M Jellouli  6   7   8   9   10 , R Maamouri  7   8   9   10 , A Talbi  8   9   10 , H Skhiri  9   10   11 , T Gargah  6   7   8   9   10
Affiliations
Case Reports

Acute renal failure in a 7-year-old boy: do not miss rare and treatable cause

A Boussetta et al. J Nephrol. 2022 Jul.
No abstract available

Keywords: Acute renal failure; Complement system; Thrombotic micronangiopathy; cobalamin C defeciency.

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References

    1. Martinelli D, Deodato F, Dionisi-Vici C (2011) Cobalamin C defect: natural history, pathophysiology and treatment. J Inherit Metab Dis 34:127–135 - DOI
    1. Grangé S, Bekri S, Artaud-Macari E et al (2015) Adult-onset renalthrombotic microangiopathy and pulmonary arterial hyper-tension in cobalamin C deficiency. Lancet 386:1011–1012 - DOI
    1. 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 - DOI
    1. 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 - DOI
    1. 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 - DOI

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