TY  - CHAP
M1  - Book, Section
TI  - Niemann-Pick Disease
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Group  of  rare  inherited  disorders  of  fat  metabolism  with  varying  degrees  of  lipid  storage  and  foam  cell  infiltration  in  tissues.  Clinical  features  include  jaundice,  progressive  loss  of  motor  skills,  feeding  difficulties,  learning  disabilities,  and  hepatosplenomegaly.  Lysosomal  storage  disorder  caused  by  deficient  activity  of  the  enzyme  acid  sphingomyelinase  (Types  A  and  B)  or  due  to  defective  function  in  cholesterol  transport  (Type  C).  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164080305
ER  -