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[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system

J Biol Chem (1992) 267:1498797

The staff at The Child Development Center has been able to devise various methods to mix, hide, and otherwise sneak the potion into our unsuspecting (but very clever) patients

Together, they address both the cause (DHT-driven miniaturization) and the environment (scalp and follicle regeneration)

Results accumulate gradually, particularly with consistent use

Reduction of Fine Lines and Wrinkles GHK-Cu stimulates collagen and glycosaminoglycan production, improving the appearance of photoaging