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5-Oxoprolinase deficiency Disease name 5-Oxoprolinase deficiency (OMIM 260005) Definition and diagnostic criteria 5-Oxoprolinase deficiency is a very rare autosomal recessive disease characterized by 5-oxoprolinuria and very heterogeneous clinical presentation (renal stone formation, enterocolitis, mental retardation, neonatal hypoglycemia, microcytic anemia and microcephaly)

Rare allergic reactions (particularly in individuals sensitive to sulfa, due to methionine)

It helps neutralize free radicals, supports liver detoxification, andmost importantly for skincareinterferes with melanin production, leading to a brighter and more even-toned complexion over time

When we say Extra Strength - we mean it

TOF, time-of-flight