FUNDRAISERS

PKU Walk
May 7, 2011
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Join the Tennessee PKU Foundation for their 5th Annual Walk for PKU. All monies raised will go to support PKU Research.
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.
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Venue Info
3777 Nolensville Road
Nashville, TN 37211 -
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Info Phone: (615) 833-1534
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Dates:
May 7, 2011Times:
Saturday 9:00am
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