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 2021/03/02 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.