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Phenylketonuria(PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the enzyme phenylalanine hydroxylase (PAH). This enzyme is necessary to metabolize the amino acid phenylalanine to the amino acid tyrosine. When PAH is deficient, phenylalanine accumulates and is converted into phenylketones, which are detected in the urine. Left untreated, this condition can cause problems with brain development, leading to progressive mental retardation and seizures. Wikipedia
| Knoxville Walk for PKU 2010 |
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| Written by Bryon McDowell | |
| Thursday, 08 July 2010 | |
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Checkout the pictures from the Knoxville Walk for PKU!                            |
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| Last Updated ( Thursday, 08 July 2010 ) |
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Become famous, send us your pictures!
Donations can be mailed to:
Tennessee PKU Foundation
P.O. Box 681914
Franklin, TN 37068
