Phenylketonuria (pronounced fee-nill-key-toe-NURR-ee-uh) or PKU is
a rare, inherited metabolic disorder. Each year, approximately 1 in
14,000 newborn babies are diagnosed with PKU. If you have PKU, your
body cannot break down, or metabolize, the essential amino acid,
phenylalanine (Phe). Amino acids are the building blocks of
protein. The primary treatment for PKU is a special metabolic
formula and the restriction of foods high in Phe (protein), such as
meats, cheeses, milk, bread and pasta. Life-long dietary compliance
is a critical component for proper growth and development in
children and quality of life in adults. We hope Penny The Penguin
can help your child on this "diet for life" journey.
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