RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164070585
T1 Gaucher Disease
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164070585
RD 2024/10/07
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.