TY  - CHAP
M1  - Book, Section
TI  - Gaucher Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Most  common  inherited  lipid  storage  disease.  It  is  particularly  common  in  Ashkenazi  Jewish  people.  Characterized  by  accumulation  of  glucocerebrosides  (derived  from  red  blood  cells)  in  many  tissues,  especially  the  macrophages  in  the  bone  marrow.  Attention  should  be  given  to  hematological  parameters  in  particular  with  children  with  mild,  nonneuronopathic  Type  I  and  severe  neuronopathic  Type  III  Gaucher  disease  in  an  attempt  to  minimize  postoperative  bleeding,  the  most  serious  complication.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164070585
ER  -