Background: Atypical haemolytic uremic syndrome (aHUS) is often associated with a high risk of disease recurrence and subsequent graft loss after isolated renal transplantation. Evidence-based recommendations for a mutation-based management after renal transplantation in aHUS caused by a combined mutation with complement factor I (CFI) and membrane cofactor protein CD46 (MCP) are limited. Case-diagnosis/Treatment: We describe a 9-year-old boy with a first manifestation of aHUS at the age of 9months carrying combined heterozygous mutations in the CFI and MCP genes. At the age of 5years, he underwent isolated cadaveric renal transplantation. Fresh frozen plasma was administered during and after transplantation, tapered and finally stopped aft...
Hemolytic uremic syndrome (HUS) is a disease of microangiopathic hemolytic anemia, thrombocytopenia ...
Background Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (T...
4 p.-1 fig.aHUS is a rare disease characterized by episodes of TMA that frequently progresses to CKD...
Complement factor H (CFH)-associated hemolytic uremic syndrome (HUS) is a genetic form of atypical H...
Pathogenic gain-of-function variants in complement Factor B were identified as causative of atypical...
International audienceAtypical hemolytic and uremic syndrome (aHUS) is a severe disease strongly ass...
Atypical hemolytic uremic syndrome (aHUS) is a rare disease of microangiopathic hemolytic anemia, th...
International audienceMutations in factor H (CFH), factor I (IF), and membrane cofactor protein (MCP...
Risk for atypical hemolytic uremic syndrome (aHUS) recurrence after renal transplantation is low wit...
BACKGROUND: Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (...
Mutations in the complement factor H (CFH) gene are frequently associated with atypical hemolytic ur...
Background and objectives: A male infant with a family history of thrombotic microangiopathy develop...
Atypical haemolytic uraemic syndrome (aHUS) is a rare, life-threatening, chronic, genetic disease du...
Disorders in the regulation of the alternate complement pathway often resultin complement-mediated d...
Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (THBD), C3 an...
Hemolytic uremic syndrome (HUS) is a disease of microangiopathic hemolytic anemia, thrombocytopenia ...
Background Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (T...
4 p.-1 fig.aHUS is a rare disease characterized by episodes of TMA that frequently progresses to CKD...
Complement factor H (CFH)-associated hemolytic uremic syndrome (HUS) is a genetic form of atypical H...
Pathogenic gain-of-function variants in complement Factor B were identified as causative of atypical...
International audienceAtypical hemolytic and uremic syndrome (aHUS) is a severe disease strongly ass...
Atypical hemolytic uremic syndrome (aHUS) is a rare disease of microangiopathic hemolytic anemia, th...
International audienceMutations in factor H (CFH), factor I (IF), and membrane cofactor protein (MCP...
Risk for atypical hemolytic uremic syndrome (aHUS) recurrence after renal transplantation is low wit...
BACKGROUND: Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (...
Mutations in the complement factor H (CFH) gene are frequently associated with atypical hemolytic ur...
Background and objectives: A male infant with a family history of thrombotic microangiopathy develop...
Atypical haemolytic uraemic syndrome (aHUS) is a rare, life-threatening, chronic, genetic disease du...
Disorders in the regulation of the alternate complement pathway often resultin complement-mediated d...
Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (THBD), C3 an...
Hemolytic uremic syndrome (HUS) is a disease of microangiopathic hemolytic anemia, thrombocytopenia ...
Background Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (T...
4 p.-1 fig.aHUS is a rare disease characterized by episodes of TMA that frequently progresses to CKD...