Tianyi Wang* Author Affiliations Ritsumeikan Global Innovation Research Organization, University, Japan Received: February 17, 2022 | Published: 28, Corresponding author: Wang, 1-1-1 Noji-higashi, Kusatsu, Shiga, DOI: 10.26717/BJSTR.2022.42.006720

HEDIAK (1952) observed anomalous granulations in peripheral blood and bone marrow leukocytes of a four-year-old girl. Several investigators have since reported similar granules in leukocytes of both male and female patients from different parts of the world. While there have been some differences reported in the various cases, the composite picture of the syndrome as described by several invest...

Chediak-Higashi syndrome (CHS) is a rare autosomal recessive immunodeficiency disease characterized by frequent infections, hypopigmentation, progressive neurologic deterioration and hemophagocytic lymphohistiocytosis (HLH), known as the accelerated phase. There is little experience in the accelerated phase of CHS treatment worldwide. Here, we present a case of a 9-month-old boy with continuous...

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