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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)

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If the desired research dose is 2,500mcg, the calculator indicates a draw of 0.5mL (50 units)

Anaheim Medical Group prioritizes patient comfort and safety throughout the IV Therapy process, ensuring that each session is conducted with utmost care and attention to detail