Atypical hemolytic-uremic syndrome due to complement factor I mutation
نویسندگان
چکیده
منابع مشابه
Atypical hemolytic-uremic syndrome due to complement factor I mutation
Atypical hemolytic-uremic syndrome (aHUS) is a rare disease of complement dysregulation leading to thrombotic microangiopathy (TMA). Renal involvement and progression to end-stage renal disease are common in untreated patients. We report a 52-year-old female patient who presented with severe acute kidney injury, microangiopathic hemolytic anemia, and thrombocytopenia. She was managed with stero...
متن کاملPostoperative Atypical Hemolytic Uremic Syndrome Associated with Complement C3 Mutation
Atypical hemolytic uremic syndrome (aHUS) can be distinguished from typical or Shiga-like toxin-induced HUS. The clinical outcome is unfavorable; up to 50% of affected patients progress to end-stage renal failure and 25% die during the acute phase. Multiple conditions have been associated with aHUS, including infections, drugs, autoimmune conditions, transplantation, pregnancy, and metabolic co...
متن کاملAtypical hemolytic uremic syndrome due to factor H autoantibody.
Atypical hemolytic uremic syndrome (aHUS) is a disease caused by pathologies in the alternative complement system. The prevalence of aHUS is 10% of all aHUS cases. The subgroup of aHUS designated as DEAP (DEficiency of CFHR Proteins and CFH Autoantibody Positive)-HUS because of autoantibody to complement factor H (CFH) and CFH-related protein deficiency is seen very rarely, and the prevalence i...
متن کاملMutations in complement factor I predispose to development of atypical hemolytic uremic syndrome.
Mutations in the plasma complement regulator factor H (CFH) and the transmembrane complement regulator membrane co-factor protein (MCP) have been shown to predispose to atypical hemolytic uremic syndrome (HUS). Both of these proteins act as co-factors for complement factor I (IF). IF is a highly specific serine protease that cleaves the alpha-chains of C3b and C4b and thus downregulates activat...
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ژورنال
عنوان ژورنال: World Journal of Nephrology
سال: 2017
ISSN: 2220-6124
DOI: 10.5527/wjn.v6.i6.243