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Alternative Pathway of complement assay to diagnose atypical HUS and other disorders of complement activation

Atypical hemolytic uremic syndrome (aHUS) is a rare microangiopathic hemolytic anemia (MAHA) that often leads to renal failure, stroke and premature death(1). In most cases the disease is caused by genetic mutation in one of more than 6 genes that leads to increased activation of the alternative pathway of complement. Currently there is no good diagnostic...

Published: 3/13/2025 | Inventor(s): Robert Brodsky

Keywords(s): aHUS, Assay, Atypical Hemolytic-Uremic Syndrome, Clinical Diagnostics, Disease Indication, Genetic Disorders, In Vitro Diagnostics

Category(s): Clinical and Disease Specializations, Clinical and Disease Specializations > Cardiovascular, Clinical and Disease Specializations > Rare Diseases, Technology Classifications > Diagnostics > In Vitro Diagnostics, Technology Classifications > Research Tools > Assays, Technology Classifications > Diagnostics, Clinical and Disease Specializations > Genetic Diseases, Technology Classifications > Research Tools, Clinical and Disease Specializations > Genetic Diseases > Atypical Hemolytic-Uremic Syndrome