5-oxoprolinemia | definition of 5-oxoprolinemia by Medical dictionary
glutathione synthetase deficiency (redirected from 5-oxoprolinemia)
glu·ta·thi·one syn·the·tase de·fi·cien·cy
an inborn error of metabolism associated with massive urinary excretion of 5-oxyproline, elevated levels of 5-oxyproline in the blood and cerebrospinal fluid, severe metabolic acidosis, tendency toward hemolysis, and defective central nervous systems function. Glutathione synthetase deficiency has been reported as a generalized condition or with a deficiency restricted to erythrocytes.
glutathione synthetase deficiency A rare autosomal recessive inborn error of metabolism dur to a mutation in the gene for glutathione synthetase. There are low levels of GLUTATHIONE, raised blood acidity, a tendency to red cell breakdown (haemolysis) and excretion of large quantities of 5-oxoproline in the urine. 5-oxoproline is a stage in the gamma-glutamyl cycle by which amino acids are transported. The antioxidant vitamin E has been used to treat cases.
References in periodicals archive
causing elevated anion gap metabolic acidosis in the setting of acetaminophen use.