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• W2003154924 abstract "Atypical hemolytic uremic syndrome (aHUS) is a rare disease of microangiopathic hemolytic anemia, thrombocytopenia, and predominant renal impairment. It is characterized by the absence of Shiga toxin-producing bacteria as a triggering factor. During the last decade, aHUS has been demonstrated to be a disorder of the complement alternative pathway dysregulation, as there is a growing list of mutations and polymorphisms in the genes encoding the complement regulatory proteins that alone or in combination may lead to aHUS. Approximately 60% of aHUS patients have so-called ‘loss-of-function’ mutations in the genes encoding the complement regulatory proteins, which normally protect host cells from complement activation: complement factor H (CFH), factor I (CFI) and membrane cofactor protein (MCP or CD46), or have ‘gain-of-function’ mutations in the genes encoding the complement factor B or C3. In addition, approximately 10% of aHUS patients have a functional CFH deficiency due to anti-CFH antibodies. Recent advances in understanding the pathogenesis of aHUS have led to a revised classification of the syndrome. Normal plasma levels of CFH and CFI do not preclude the presence of a mutation in these genes. Further, genotype-phenotype correlations of aHUS have clinical significance in predicting renal recovery and transplant outcome. Therefore, it is important to make a comprehensive analysis and perform genetic screening of the complement system in patients with aHUS to allow a more precise approach, especially before transplantation. This may also provide opportunities for more specific treatments in the near future, as complement inhibition could represent a therapeutic target in these patients who have a considerably poor prognosis in terms of both mortality and progression to end-stage renal disease and a great risk of disease recurrence after transplantation." @default.
• W2003154924 created "2016-06-24" @default.
• W2003154924 creator A5032312810 @default.
• W2003154924 creator A5040957114 @default.
• W2003154924 creator A5078915790 @default.
• W2003154924 date "2010-01-14" @default.
• W2003154924 modified "2023-10-16" @default.
• W2003154924 title "Atypical Hemolytic Uremic Syndrome: Update on the Complement System and What Is New" @default.
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• W2003154924 doi "https://doi.org/10.1159/000276545" @default.
• W2003154924 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20090363" @default.
• W2003154924 hasPublicationYear "2010" @default.
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