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  • Molecular assay reagents intended to identify gene variants associated with hemophagocytic lymphohistiocytosis, a hereditary syndrome associated with elevated numbers of activated lymphocytes that leads to chronic fevers and damage to the liver, spleen, bone marrow, and brain. Genetic variants at multiple loci have been associated with various forms of hemophagocytic lymphohistiocytosis. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hemophagocytic lymphohistiocytosis-associated loci simultaneously.
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