RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58062363
T1 Alpha-Mannosidosis
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=58062363
RD 2020/06/05
AB Characterized  by  Hurler-like  facial  features,  moderate-to-severe  mental  retardation,  recurrent  pulmonary  infections,  reduced  hearing,  immunodeficiency,  skeletal  abnormalities,  and  primary  central  nervous  system  disease,  mainly  ataxia.  It  is  also  frequently  associated  with  corneal  opacities,  aseptic  destructive  arthritis,  and  metabolic  myopathy.  Communicating  hydrocephalus  can  occur  in  individuals  of  any  age.  Cardiac  and  renal  complications  are  rarely  encountered.  Alpha-mannosidosis  is  insidiously  progressive.  Individuals  may  live  into  the  sixth  decade.