“…Absence of inclusions in granulocytes on peripheral blood examination and hair microscopy findings confirmed the diagnosis of GS and ruled out Chediak Higashi syndrome (8). Consistent with symptoms described in subtype 2, this child also shared features like fever, pallor, jaundice, hepatosplenomegaly, and fulfilled five criteria of HLH -fever, pancytopenia, splenomegaly, raised ferritin (1,053 ng/mL) and hypertriglyceridemia (triglycerides-311 mg/dL) / hypofibrinogenemia (108 mg/dL).…”