RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164061181
T1 Oculocutaneous Albinism Type VIB: Chediak-Higashi Syndrome (CHS)
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164061181
RD 2024/04/24
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.