Phenylketonuria

What is phenylketonuria, the main symptoms and how is the remedy performed?

Phenylketonuria is a rare genetic disease characterized by the presence of a mutation responsible for altering the function of an enzyme in the body responsible for converting the amino acid phenylalanine into tyrosine, leading to the accumulation of phenylalanine in the blood and which at high concentrations is toxic to the body, which can cause

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