RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164067887
T1 Diaminopentanuria
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164067887
RD 2024/04/19
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.