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Hypoglycemia (the primary acute risk) In the Increlex program, hypoglycemia was reported in 30 of 71 subjects (42%)
One type of mutation, found almost exclusively in people of Ashkenazi Jewish heritage, affects the autonomic and sensory nervous system development causing familial dysautonomia (FD ) Another mutation causes an increased level of phenylalanine (Phe) in the bloodstream resulting in a metabolic disorder called phenylketonuria (PKU)
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CL Answer How can I avoid aconite a toxin in Aconitum supplements
Some researchers alternate between the two, using AHK-Cu one week and GHK-Cu the next
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