TY  - CHAP
M1  - Book, Section
TI  - Alpha-Mannosidosis
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
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.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164061461
ER  -