RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58080724
T1 I-Cell 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=58080724
RD 2024/04/20
AB I-cell  disease  stands  for  inclusion  cell  disease.  It  is  a  genetically  inherited  lysosomal  storage  disease  clinically  similar  to  Hurler  syndrome  (without  mucopolysaccharides)  and  originally  characterized  by  the  presence  of  intracytoplasmic  inclusions  in  fibroblasts  (“inclusion  cells”  or  “I  cells”).