TY - CHAP M1 - Book, Section TI - I-Cell Disease A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. Y1 - 2006 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - I-cell disease stands for inclusion cell disease. It is a genetically inherited lysosomal storage disease clinically similar to Hurler syndrome (without mucopolysaccharides) and originally characterized by the presence of intracytoplasmic inclusions in fibroblasts (“inclusion cells” or “I cells”). SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58080724 ER -