Phenylketonuria (PKU)
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Information on PKU
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Phenylketonuria - Wikipedia, the free encyclopedia
Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the enzyme hepatic phenylalanine hydroxylase. ...
en.wikipedia.org/wiki/Phenylketonuria
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PKU - 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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PKU - Phenylketonuria
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MedlinePlus: Phenylketonuria
Phenylketonuria (PKU) is a genetic disorder in which the body can't process part of a protein called phenylalanine (Phe). Phe is in almost all foods. ...
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.
www.mayoclinic.com/health/phenylketonuria/DS00514
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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, ...
www.medicinenet.com/phenylketonuria/article.htm
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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
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,
www.answers.com/topic/phenylketonuria
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MedlinePlus Medical Encyclopedia: Phenylketonuria
Definition, causes, symptoms and treatment. ... Phenylketonuria (PKU) is inherited, which means it is passed down through families. ...
www.nlm.nih.gov/medlineplus/ency/article/001166.ht...
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OMIM - PHENYLKETONURIA; PKU
MIM #261600 ? Text ? Description ? Clinical Features ? Biochemical Features ? Inheritance ? Mapping ? Molecular Genetics ? Genotype/Phenotype Correlations ...
www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261600
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Take Control of PKU (Phenylketonuria)
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