See Also: hyperglycinaemia(medicine)
Herbal medicine (botanical medicine, herbology, phytomedicine)(health)
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-acetylglucosaminyl transferase(medicine)
beta-1,3-galactosyl-0-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase(medicine)
UDP-GalNAc-beta-galactose beta 1,4-N-acetylgalactosaminyltransferase(medicine)
beta-1,4-mannosyl-glycoprotein beta-1,4-N-acetylglucosaminyltransferase(medicine)
Medicine Lodge Memorial Hospital- Medicine Lodge(health)
beta-n-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase(medicine)
Beta-hydroxy-beta-methylglutaryl-CoA(medicine)
androst-5-ene-3 beta,17 beta-diol(medicine)

beta-normal (medicine) and hyperglycinaemia (medicine)


beta-normal (medicine)


beta-normal
<radiobiology> Beta-N, the normalised beta, is beta relative to the beta limit.


hyperglycinaemia (medicine)


hyperglycinaemia


Elevated plasma glycine concentration.

Ketotic hyperglycinaemia, an inherited metabolic defect which results from a deficiency of propionyl Coenzyme A carboxylase, the enzyme that converts propionate to methylmalonate; the enzyme requires biotin as a cofactor; clinically, affected infants have overwhelming illness, with lethargy, metabolic acidosis with ketosis, hypotonia; coma and seizures typically develop with early death; propionic acid is markedly elevated in plasma and urine; there is also hyperammonaemia, and elevated levels of Other metabolites as well, include glycine, hence the original name for the syndrome.

Synonym: methylmalonic acidemia, propionic acidemia.

Nonketotic hyperglycinaemia, an inborn error of glycine metabolism, resulting from a defect in the glycine cleavage enzyme system; characteristically overwhelming disease in the newborn period, with coma, seizures and death, or, less often, gradual onset with failure to thrive, focal seizures, and mental retardation; there is massive elevation of plasma glycine, with increased levels in cerebrospinal fluid and urine; plasma hyperosmolality, severe dehydration occur without ketoacidosis; autosomal recessive inheritance.