TY - CHAP M1 - Book, Section TI - Glycogen Storage Disease Type II A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Inborn error of metabolism that results from the deficiency of acid alpha-glucosidase, a lysosomal hydrolase. The three variants are infantile, juvenile, and adult onset. In the classic infantile form (Pompe disease), cardiomyopathy and muscular hypotonia are the cardinal features. In the juvenile and adult forms, involvement of skeletal muscles dominates the clinical presentation. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58078034 ER -