- 0 Comments
- BLOG Neurological / Psychological
Phenylketonuria (PKU) emanates from an autosomal recessive deficiency of phenylalanine hydroxylase; an enzyme responsible for converting phenylalanine to a neurotransmitter precursor known as tyrosine.1 Left untreated, PKU can produce irreversible neurological damage to include developmental challenges.1(47) Thus, rapid interventions upon diagnosis is critical to avoid such pathophysiological outcomes. A standard intervention includes avoidance of proteins rich […]
Read More