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Methionine malabsorption syndrome

Oast house urine disease (methionine malabsorption syndrome, 2-hydroxybutyric aciduria) Methionine, 2-hydroxybutyric, phenylpyruvic and the branched-chain keto acids especiaUy 2-oxoisovaleric Methionine malabsorption (amino acid-transport defect) (Chapter 16)... [Pg.216]

Cyanocobalamin A cofactor required for essential enzymatic reactions that form tetrahydrofolate, convert homocysteine to methionine, and metabolize l-methylmalonyl-CoA Adequate supplies are required for amino acid and fatty acid metabolism, and DNA synthesis Treatment of vitamin B12 deficiency, which manifests as megaloblastic anemia and is the basis of pernicious anemia Parenteral vitamin B12 is required for pernicious anemia and other malabsorption syndromes Toxicity No toxicity associated with excess vitamin B12... [Pg.749]


See other pages where Methionine malabsorption syndrome is mentioned: [Pg.206]    [Pg.2]    [Pg.405]    [Pg.440]    [Pg.206]    [Pg.2]    [Pg.405]    [Pg.440]    [Pg.30]    [Pg.193]    [Pg.31]   
See also in sourсe #XX -- [ Pg.2 , Pg.216 , Pg.405 ]




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Malabsorption

Malabsorption syndromes

Methionine malabsorption

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