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31
Phenylketonuria (PKU)-Topic Overview (Search Map)

Phenylketonuria (PKU) is a genetic disorder in which a baby lacks or has very low levels of the enzyme phenylalanine hydroxylase (PAH)


32
Children's PKU Network - What is PKU? (Search Map)

Phenylketonuria (PKU) is a genetic inborn error of metabolism that is detectable during the first days of life with appropriate blood testing (newborn screening) ...


33
PKU Action Group - Seattle, Washington (Search Map)

The University of Washington PKU (phenylketonuria)clinic web site provides resources to families of children with PKU and professionals who work with those children.


34
Phenylketonuria (Search Map)

PKU is caused by a mutation in a gene on chromosome 12. The gene codes for a protein ... PKU is an autosomal recessive disorder, meaning that you need to ...


35
Phenylketonuria - MayoClinic.com (Search Map)

People with phenylketonuria (PKU) — babies, children and adults — need to follow a diet that limits phenylalanine, which is found mostly in high-protein foods. ...


36
Home (Search Map)

PKU Perspectives offers a unique and growing selection of economical low protein food products for a PKU diet and other metabolic disorders or medical ...


37
Phenylketonuria (PKU) - Topic Overview - Yahoo! Health (Search Map)

If PKU is treated soon after birth, all or most of these problems can usually be prevented. ... Early symptoms of PKU include a musty odor to the skin, hair, and urine. ...


38
New Parents' (Search Map)

child with phenylketonuria (called PKU), with PKU and its treatment. ... also help to orient you to the PKU clinic and the people there who will help ...


39
Basic PKU Biochem (Search Map)

Defects in Biopterin Metabolism and PKU. Defects in the regeneration of the cofactor tetrahydobiopterin (BH4) account for a small fraction of PKU cases. ...


40
Phenylketonuria (PKU) - Better Health Channel. (Search Map)

Phenylketonuria (PKU) is an inherited disorder. It occurs when the body cannot break down a substance in food, called phenylalanine. ...


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