The syndrome identified as hemophagocytic lymphohistiocytosis (HLH) poses a rather difficult challenge to the physician. HLH was initially described as a familial disorder. 1 which was later associated with various genetic defects that affect the cytotoxic machinery of CD8+ T and NK cells. 2 but it also occurs sporadically. https://minidsreamers.shop/product-category/long-sleeve-tops/