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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. ...
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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 ...
www.nlm.nih.gov/medlineplus/phenylketonuria.html
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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) Signs, Symptoms, Causes, and Prognosis on ...
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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