The patient is a 33 year old woman at 31 weeks gestation with twins who presented to the
ER complaining of shortness of breath, headache, and blurry vision. The patient's …

Atypical HUS (aHUS) is a disease of complement dysregulation. In~ 50% of patients
mutations have been described in the genes encoding the complement regulators factor H …

Atypical hemolytic uremic syndrome (aHUS) is a major thrombotic microangiopathy (TMA). A
TMA is recognized by the laboratory signs of microangiopathic hemolysis, as indicated by …

Objective Although the definitive diagnosis of atypical hemolytic uremic syndrome (aHUS)
depends on a genetic analysis for the complement factors, such a genetic analysis is time …

Atypical hemolytic uremic syndrome is a rare form of thrombotic microangiopathies resulting
from various genetic mutations of the complement factors. Thrombotic microangiopathies …

Hemolytic uremic syndrome (HUS) is a major thrombotic microangiopathy, identified by triad
of laboratory evidence of hemolytic anemia, thrombocytopenia, and renal impairment …

Background: Atypical Haemolytic Uremic Syndrome (aHUS) is a genetic or acquired
disorder of regulatory component of the complement system. It is associated with mutations …

The atypical Hemolytic Uremic Syndrome (aHUS) is a rare thrombotic microangiopathy
leading to end stage renal disease in approximately 60% of patients. Over the last decade, a …

Introduction: Pregnancy-related acute kidney injury is the most common cause of renal
cortical necrosis (RCN). Atypical hemolytic uremic syndrome (aHUS) as a cause of RCN in …

Atypical hemolytic uremic syndrome (aHUS) is a rare syndrome of hemolysis,
thrombocytopenia, and renal insufficiency. Genetic mutations in the alternate pathway of …