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Glutathione synthetase deficiency is an autosomal recessive disorder that was first diagnosed in 1970 in a teenager with a slowly progressive neurologic disorder and markedly elevated excretion of 5-oxoproline in the urine, as well as a history of unexplained jaundice at birth and a history of chronic metabolic acidosis

doi: 10.1016/J.MTCHEM.2021.100673 56 GmezM

This anti-inflammatory action decreases oxidative stress across multiple organ systems, supporting its use in experimental protocols for chronic inflammation and metabolic disorders

Dai et al., 2024a

The interplay of uterine health and obesity: A comprehensive review