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Phenylketonuria, often abbreviated as PKU, is a rare genetic disorder that affects how the body processes a particular amino acid called phenylalanine. Discovered in the 1930s, PKU has since been a focal point in understanding genetic metabolic disorders and their management. This blog post delves into the basics of PKU, its symptoms, diagnosis, and treatment options, providing a comprehensive overview for anyone looking to learn more about this condition. https://lnkd.in/gAuZs9Ai #BhaloTheko

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