Atypical HUS with multiple complement system mutations triggered by synthetic psychoactive drug abuse: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-023-01646-4.pdf
Reference17 articles.
1. Taylor C, Machin S, Wigmore SJ, Goodship TH (2010) Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom. Br J Haematol 148:37–47. https://doi.org/10.1111/j.1365-2141.2009.07916.x
2. Siomou E, Gkoutsias A, Serbis A, Kollios K, Chaliasos N, Fremeaux-Bacchi V (2016) aHUS associated with C3 gene mutation: a case with numerous relapses and favorable 20-year outcome. Pediatr Nephrol 31:513–517. https://doi.org/10.1007/s00467-015-3267-3
3. Raina R, Krishnappa V, Blaha T, Kann T, Hein W, Burke L, Bagga A (2019) Atypical Hemolytic-uremic syndrome: an update on pathophysiology, diagnosis, and treatment. Ther Apher Dial 23:4–21. https://doi.org/10.1111/1744-9987.12763
4. Loirat C, Frémeaux-Bacchi V (2011) Atypical hemolytic uremic syndrome. Orphanet J Rare Dis 6:60. https://doi.org/10.1186/1750-1172-6-60
5. Caprioli J, Noris M, Brioschi S et al (2006) Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 108:1267–1279. https://doi.org/10.1182/blood-2005-10-007252
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1. The Rationale of Complement Blockade of the MCPggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review;International Journal of Molecular Sciences;2023-08-22
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