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HLH Pathogenesis of HLH HLH is a rare and potentially life-threatening hyperinflammatory response syndrome characterized by dysregulated activation of cytotoxic T-lymphocytes, NK-cells, and macrophages resulting in a cascade of hypercytokinemia and immune-mediated harm to various organ systems (Fig

Precision Testing Includes EBV, CMV, HSV-1/2, HHV-6/7, and Streptococcal Apathogens known to impact neurological immune activity

Therefore, it is imperative to explore the metabolic characteristics of TNBC to identify novel therapeutic targets

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The body requires time to replenish depleted stores, regenerate red blood cells, and repair neurological damage caused by prolonged deficiency