Phenylketonuria
Inside the condition centers at ThirdAge.com you can learn more about all conditions, including Phenylketonuria. Research the condition by topics such as causes, symptoms, diagnosis, complications, and more. Learn how to take action with information on Phenylketonuria treatment options, prevention methods, support groups, and more. Select a topic below for more information.
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What is Phenylketonuria?
Phenylketonuria (PKU) is an inherited metabolic disorder in which a person does not have the liver enzyme needed to break down phenylalanine, an amino acid found in proteins and some artificial sweeteners. Without this enzyme, phenylalanine can build up in the blood and become toxic to the brain. Approximately 1 in 15,000 infants in the US is born with PKU.
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 Risk Factors Are you at risk of getting Phenylketonuria? Inside you'll find known risk factors for the condition. |
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 Diagnosis How will your doctor diagnose you with this condition? Learn about the tests, process, and more. |
 Complications Can this condition lead to other health problems? Learn more about the known complications. |
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 Screening Learn more about the specific tests or exams given by your doctor to screen for Phenylketonuria. |
 Medications What medications offer relief or help with this condition? Are there side effects? Risks? Learn more. |
 Prevention How can you prevent Phenylketonuria? Read what the medical community suggests for prevention methods. |
 Care Learn more about the day to day care of this condition. Changes to your activity, diet, exercise, and more. |
 Find a Doctor Do you need to contact a doctor about Phenylketonuria? Select a location to find a specialist in your area. |
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