Rare Medical News

5 Facts you should know about

Atypical hemolytic uremic syndrome

fivefacts-light.svg

1

AHUS is usually caused by chronic, uncontrolled activation of the complement system.

2

The disease affects both children and adults and is characterized by systemic thrombotic microangiopathy.

3

Clinical signs and symptoms of complement-mediated TMA can include abdominal pain, confusion, fatigue, edema, nausea/vomiting, and diarrhea.

4

Patients with aHUS often present with an abrupt onset of systemic signs and symptoms such as acute kidney failure, hypertension, myocardial infarction, stroke, or pancreatitis.

5

AHUS can be inherited or acquired and does not appear to vary by race, gender, or geographic area.

Rare Medical News