RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58077506
T1 Gangliosidosis (GM1) Type I
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=58077506
RD 2023/10/03
AB Lysosomal  storage  disease.  Affected  patients  have  clinical  features  resembling  those  of  mucopolysaccharidoses  types  I  and  VI  but  without  mucopolysacchariduria.  Clinical  features  include  joint  stiffness,  scoliosis,  and  skeletal  dystrophy.  Valvular  heart  diseases  are  present,  of  which  aortic  insufficiency  is  the  most  common.  Obstructive  sleep  apnea  is  frequent,  and  50%  of  reported  cases  have  mild  mental  retardation.