Tennessee PKU Foundation News
| ||||||||||||||||||||||
| ||||||||||||||||||||||
More...
| ||||||||||||||||||||||
| << Start < Prev 1 2 3 4 5 6 7 Next > End >> | ||||||||||||||||||||||
| Results 1 - 4 of 27 | ||||||||||||||||||||||
Main Menu
| Home |
| News |
| News Feeds |
| Forums |
| Calendar of Events |
| Links |
| Search |
| FAQs |
| Contact Us |
What is PKU?
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
Calendar of Events
Login Form
Member Spotlight
Abigail McDowell
Become famous, send us your pictures!
Donate
Donations can be mailed to:
Tennessee PKU Foundation
P.O. Box 681914
Franklin, TN 37068
