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Individuals who have deletions of the entire NF1 gene have an increased risk of facial dysmorphism, mental retardation, early appearance of neurofibromas, and the presence of plexiform neurofibromas.1 In addition, individuals who have a specific 3 base pair in-frame deletion in exon 17 of the NF1 gene may have caf-au-lait spots, intertriginous freckling and Lisch nodules, but do not develop cutaneous, subcutaneous or plexiform neurofibromas

The fluorescence values of the solution (Ex = 560 nm, Em = 595 nm) were measured at predetermined time points using a microplate reader (Synergy 2, BioTek Instruments Inc, USA)

Y.GratacsE.CarrascoP.ClotetJ.UreaJ.SerraD.et al (2008)

In Summary, while early research in animal models points toward potential healing and regenerative properties for BPC-157, the complete lack of well-designed human clinical trials makes it a gamble