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Hyperuricemia glycogen storage disease

Individuals with a glucose-6-phosphatase (G-6-P —> Glucose, in the liver) deficiency develop a glycogen storage disease. This condition results in hypoglycemia, low blood sugar, accumulation of lactic acid and ketones. Distal kidney tubule excretion of uric acid is inhibited and hyperuricemia (XS uric acid) and gout results. [Pg.382]

Two reports of a new genetic abnormality in primary gout associated with elevated intracellular PP-ribose-P levels and increased PP-ribose-P synthetase have been described in detail at this meeting. The hyperuricemia of glycogen storage disease (Type 1) caused by deficient glucose-6-phosphatase, has been shown by a... [Pg.114]

See other pages where Hyperuricemia glycogen storage disease is mentioned: [Pg.441]    [Pg.631]    [Pg.236]    [Pg.296]    [Pg.301]    [Pg.307]    [Pg.353]    [Pg.361]    [Pg.361]   
See also in sourсe #XX -- [ Pg.361 , Pg.362 , Pg.363 , Pg.364 , Pg.365 ]

See also in sourсe #XX -- [ Pg.361 , Pg.362 , Pg.363 , Pg.364 , Pg.365 ]



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