Chapter 23: Q30P (page 829)
Why does von Gierke’s glycogen storage disease (Box 16-2) cause symptoms of gout?
Short Answer
Defective gluconeogenesis leads to high lactate levels, which results in the accumulation of uric acid.
Chapter 23: Q30P (page 829)
Why does von Gierke’s glycogen storage disease (Box 16-2) cause symptoms of gout?
Defective gluconeogenesis leads to high lactate levels, which results in the accumulation of uric acid.
All the tools & learning materials you need for study success - in one app.
Get started for freeDescribe how purine catabolism is related to SCID, muscle function, and gout.
Gout resulting from the de novo overproduction of purines can be distinguished from gout caused by impaired excretion of uric acid by feeding a patient 15N- labeled glycine and determining the distribution of 15Nin his or her excreted uric acid. What isotopic distributions are expected for each type of defect?
What is the role of thioredoxin and NADPH in the formation of deoxyribonucleotides?
A nucleotide derivative that may have intracellular signaling activity is synthesized fromby the removal of the nicotinamide group and addition of an acetyl group at the 2′ position of the ribose attached to ADP. Draw its structure.
Why is it important that muscle cells have low levels of glutamate dehydrogenase?
What do you think about this solution?
We value your feedback to improve our textbook solutions.