31 top medical experts on Inborn Errors Fructose Metabolism across 5 countries and 3 U.S. states, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Inborn Errors Fructose Metabolism: Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Inborn Errors Carbohydrate Metabolism (1,325) and Narrower Categories: Fructose-1,6-Diphosphatase Deficiency (177), Fructose Intolerance (306).
- Clinical Trials : at least 2 including 1 Active, 1 Completed
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