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Phenylketonuria - Wikipedia, the free encyclopedia
Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the hepatic enzyme phenylalanine hydroxylase (PAH). ...
en.wikipedia.org/wiki/Phenylketonuria
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PHENYLKETONURIA (PKU)
Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to utilize the essential amino acid, phenylalanine. ...
www.medhelp.org/lib/pku.htm
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Phenylketonuria: MedlinePlus
Sep 3, 2009 ... The primary NIH organization for research on Phenylketonuria is the National Institute of Child Health and Human Development ...
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Phenylketonuria - MayoClinic.com
Phenylketonuria Comprehensive overview covers symptoms, treatment (including diet information) of this rare birth defect.
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Phenylketonuria: MedlinePlus Medical Encyclopedia
Phenylketonuria (PKU) is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine. ...
www.nlm.nih.gov/medlineplus/ency/article/001166.ht...
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Phenylketonuria - Genetics Home Reference
Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. ...
ghr.nlm.nih.gov/condition=phenylketonuria
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Phenylketonuria (PKU), an inherited disorderis an inherited disorder in which signs and symptoms vary from mild to severe such as seizures, ...
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Phenylketonuria
PHENYLKETONURIA (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. Loss of this enzyme results in ...
www.ncbi.nlm.nih.gov/disease/Phenylketo.html
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phenylketonuria: Definition from Answers.com
More about Phenylketonuria: Causes and symptoms Diagnosis Treatment Resources Phenylketonuria Definition Phenylketonuria (PKU) is a rare, inherited,
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