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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)

A 2019 rodent study in Journal of Orthopaedic Research (N = 40 rats, divided across four dose cohorts) found that systemic BPC-157 at 10 mcg/kg accelerated Achilles tendon reattachment strength by 44% versus saline controls at 14 days [4]

Enhanced Nutrient Absorption One of the primary advantages of IV vitamin therapy is its ability to bypass the digestive system, ensuring that nutrients are absorbed directly into the bloodstream

These people had previously experienced calf pain while walking, but with twice-daily IV glutathione treatment, they could walk farther without pain