RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164061461
T1 Alpha-Mannosidosis
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164061461
RD 2024/04/18
AB A  lysosomal  storage  disorder  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.  It  is  also  frequently  associated  with  corneal  opacities,  aseptic  destructive  arthritis,  and  metabolic  myopathy.  Communicating  hydrocephalus  can  occur  at  any  age.  Cardiac  and  renal  complications  are  rarely  encountered.  Alpha-mannosidosis  is  insidiously  progressive.  Individuals  may  live  into  the  sixth  decade.