phenylketonuria definition

  • noun:
    • A genetic condition when the human anatomy lacks the chemical necessary to metabolize phenylalanine to tyrosine. Kept untreated, the condition trigger mind harm and progressive mental retardation as a consequence of the accumulation of phenylalanine and its particular description services and products.
    • A metabolic disorder which individuals are lacking the liver enzyme phenylalanine hydroxylase (PAH) that will be needed to metabolize the amino acid phenylalanine.
    • an inherited disorder of k-calorie burning; not enough the enzyme necessary to switch phenylalanine into tyrosine results in a build up of phenylalanine in the body fluids that causes numerous examples of psychological deficiency

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