Atypical hemolytic uremic syndrome (aHUS) is an extremely rare disease characterized by low levels of circulating red blood cells due to their destruction (hemolytic anemia), low platelet count (thrombocytopenia) due to their consumption and inability of the kidneys to process waste products from the blood and excrete …

Living with aHUS When you have aHUS, you should work with a nephrologist (a kidney doctor), and/or a hematologist (a blood doctor) to monitor your condition. You will need to have regular blood tests to check the health of your kidneys and your platelet and red blood cell counts.

coli and is often the result of a genetic mutation. Typical hemolytic uremic syndrome (HUS) is an uncommon disease that occurs in 5 to 15 percent of individuals, especially children, who are infected by the Escherichia coli (E.

Atypical hemolytic uremic syndrome (aHUS) is an extremely rare, life-threatening, progressive disease that frequently has a genetic component. In most cases it can be effectively controlled by interruption of the complement cascade.

Hemolytic uremic syndrome (HUS) is a condition that affects the blood and blood vessels. It results in the destruction of blood platelets (cells involved in clotting), a low red blood cell count (anemia) and kidney failure due to damage to the very small blood vessels of the kidneys.

It may last as long as 7 to 10 days. What type of treatment should I expect for my child? If symptoms are mild, no treatment is needed. Sometimes, children with HUS have to stay in the hospital.

To confirm a diagnosis of HUS , your doctor is likely to perform a physical exam and recommend lab tests, including:

1. Blood tests. These tests can determine if your red blood cells are damaged.
2. Urine test. This test can detect abnormal levels of protein, blood and signs of infection in your urine.
3. Stool sample.

Hemolytic uremic syndrome (HUS) is a rare condition that can lead to kidney failure. It is a serious illness and can be fatal. But most children with the most common form of HUS recover with full kidney function.

Atypical hemolytic uremic syndrome (aHUS) is a disease that causes blood clots in small blood vessels in your kidneys and other organs. These clots keep blood from getting to your kidneys, which can lead to serious medical problems, including kidney failure. There’s no cure, but treatment can help manage the condition.

Hemolytic uremic syndrome (HUS) is a complex condition where an immune reaction, most commonly after a gastrointestinal tract infection, causes low red blood cell levels, low platelet levels, and kidney injury. Infections of the gastrointestinal tract (your stomach and intestines) are the most common cause of this syndrome.

Pediatric hemolytic uremic syndrome (HUS) occurs when tiny tubes in the kidneys become clogged with damaged red blood cells, impairing kidney function. What is Pediatric Hemolytic Uremic Syndrome (HUS)? Hemolytic uremic syndrome is a condition that causes damaged red blood cells to clog tiny tubes in the kidney, called glomeruli.

Nonspherocytic hemolytic anemia due to hexokinase deficiency (NSHA due to HK1 deficiency) is a very rare condition mainly characterized by severe, chronic hemolysis, beginning in infancy. Approximately 20 cases of this condition have been described to date.