Pentosuria
MONDO:0009846Pentosuria is an inborn error of metabolism which is characterized by the excretion of 1 to 4 g of the pentose L-xylulose in the urine per day.
Also known as: essential pentosuria, pentosuria, xylitol dehydrogenase deficiency, L-Xylulosuria, L-xylulose reductase deficiency, PNTSU
0 clinical trials for this condition and its sub-types, 0 tagged with Pentosuria itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.