RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58080235 T1 Hurler Syndrome 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=58080235 RD 2024/03/28 AB Genetically transmitted lysosomal storage disease resulting in accumulation of acid mucopolysaccharides in the central nervous system and peripheral tissues characterized by coarse facies (gargoyle-like), profound mental retardation, considerable hepatomegaly, hernias, enlarged tongue, skeletal disorders (kyphoscoliosis), dwarfism, and respiratory and cardiac impairment.