Atypical hemolytic uremic syndrome (aHUS) is an extremely rare, life-threatening, progressive disease that frequently has a genetic component. In most cases it is caused by chronic, uncontrolled activation of the complement system, a branch of the body. Atypical hemolytic uremic syndrome panel is a molecular diagnostic test that screens for CFH, CFHR3, CFHR1, CFHR2, CD46, and CFI genes.
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