Phenylketonuria (PKU) is a genetic disorder that impairs the body's ability to metabolize phenylalanine, requiring dietary management to mitigate symptoms.
Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by the inability to metabolize the amino acid phenylalanine. Individuals with PKU lack the enzyme phenylalanine hydroxylase, leading to a buildup of phenylalanine in the body. Left untreated, PKU can cause issues with brain development and other symptoms, but a low-phenylalanine diet can help manage the condition.
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