Atypical hemolytic uremic syndrome : Current Opinion in Hematology Atypical hemolytic uremic
syndrome : Current Opinion in Hematology Log in or Register Subscribe to journalSubscribe Get …

Atypical hemolytic uremic syndrome (aHUS) is a disease characterized by overactivation of
complement. Recurrence following renal transplantation is determined by a genetic …

Background. A child, who presented atypical haemolytic uraemic syndrome (aHUS) at the
age of 1 month, developed cerebral ischaemic events at the age of 10 years. Results …

We report the case of an 8-year-old girl diagnosed with atypical hemolytic uremic syndrome
(aHUS) with a complement factor B (CFB) gene mutation. aHUS is a disease of complement …

We report a case of atypical hemolytic uremic syndrome (aHUS) triggered by influenza A
(H1N1) in a 17-year-old boy with a mutation in the gene (CD46) encoding the …

In the last 10 years the knowledge of the pathophysiology of atypical hemolytic uremic
syndrome (aHUS) has substantially increased. Nevertheless, aHUS remains a severe …

Patients with some hereditary nephropathies—including autosomal dominant polycystic
kidney disease (ADPKD), Fabry disease and Alport syndrome—can progress to end-stage …

Summary Atypical Haemolytic Uraemic Syndrome (aHUS) is a thrombotic microangiopathy
that often provokes irreversible renal damage and post‐transplantation recurrence. Studies …

The hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are
rare diseases that manifest with thrombocytopenia and microangiopathic hemolytic anemia …

A male infant was diagnosed with atypical hemolytic uremic syndrome (aHUS) at the age of
5.5 months. Sequencing of the gene (CFH) encoding complement factor H revealed a …