TY - CHAP M1 - Book, Section TI - Oculocutaneous Albinism Type VIB: Chediak-Higashi Syndrome (CHS) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Autosomal recessive disorder characterized by immunodeficiency, platelet dysfunction, and partial oculocutaneous albinism. It may present with axonal and demyelinating types of peripheral neuropathy that can be associated with central nervous system disorders. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164061181 ER -