TY - CHAP M1 - Book, Section TI - Diaminopentanuria A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Genetic disorder with increased renal clearance of cystine, lysine, arginine, and ornithine caused by a dysfunction of the reabsorptive capacity of the renal tubules. In addition, defective intestinal absorption results in increased degradation of these amino acids by bacteria in the intestine. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/06 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164067887 ER -