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phenylalanine hydroxylase
How is PKU Diagnosed?
PKU is typically diagnosed through
newborn screening
programs. A blood sample is taken from the heel of the newborn and tested for high levels of phenylalanine. Early diagnosis is crucial for preventing the severe consequences of the disorder.
Frequently asked queries:
What is Phenylalanine Hydroxylase?
What Happens When PAH is Deficient?
How is PKU Diagnosed?
What is the Prevalence of PKU?
What are the Risk Factors for PKU?
What are the Treatment Options for PKU?
How is PKU Monitored?
What is the Impact of PKU on Public Health?
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