{"id":12714,"date":"2024-10-11T16:59:14","date_gmt":"2024-10-11T14:59:14","guid":{"rendered":"https:\/\/valintermed.com\/?p=12714"},"modified":"2024-10-11T16:59:14","modified_gmt":"2024-10-11T14:59:14","slug":"fenilketonuriya-fku","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/fenilketonuriya-fku\/","title":{"rendered":"Phenylketonuria (PKU)"},"content":{"rendered":"
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Phenylketonuria (PKU) is an inherited metabolic disorder caused by a deficiency of the enzyme phenylalanine hydroxylase, which results in a disorder of the metabolism of the amino acid phenylalanine. Without adequate treatment, phenylalanine levels in the body increase, which can cause severe neurological consequences and developmental disabilities. PKU is one of the most common examples of inherited metabolic disorders and requires early diagnosis and ongoing monitoring to prevent serious complications.<\/p>\n

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