TY - CHAP M1 - Book, Section TI - Niemann-Pick Disease A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Group of rare inherited disorders of fat metabolism. Clinical features include jaundice, progressive loss of motor skills, feeding difficulties, learning disabilities, and hepatosplenomegaly. Lysosomal storage disorder caused by a defect in sphingolipid metabolism and involving brain and/or viscera. There are five types of Newman-Pick disease. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/04/19 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58081734 ER -