RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58081734
T1 Niemann-Pick Disease
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58081734
RD 2024/04/23
AB Group  of  rare  inherited  disorders  of  fat  metabolism.  Clinical  features  include  jaundice,  progressive  loss  of  motor  skills,  feeding  difficulties,  learning  disabilities,  and  hepatosplenomegaly.  Lysosomal  storage  disorder  caused  by  a  defect  in  sphingolipid  metabolism  and  involving  brain  and/or  viscera.  There  are  five  types  of  Newman-Pick  disease.