RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58086820
T1 Sialidosis
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=58086820
RD 2024/04/25
AB A  genetic  neurodegenerative  disease,  divided  into  two  types.  These  conditions  are  caused  by  a  missing  enzyme  (sialidase)  that  results  in  the  accumulation  of  sialic  acid  in  the  nerve  cells.  Type  II  is  reported  in  infants  and  toddlers.