Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder characterised by uncontrolled activation of CD8+ T lymphocytes and macrophages. resulting in organ damage. While primary HLH is associated with genetic defects. secondary HLH can be triggered by infections. https://www.roneverhart.com/Sigon-s-Shelter-West-Ladder/
Scrub typhus complicating hemophagocytic lymphohistiocytosis: a case report.
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