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Alternate Name(s): PKU ...... Phenylketonuria (PKU) is a rare hereditary condition in which the amino acid phenylalanine is not properly metabolized. PKU can cause severe mental retardation if not treated.
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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. If the Phe level gets too high, it can damage the brain and cause severe mental retardation.
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Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to utilize the essential amino acid, phenylalanine. Amino acids are the building blocks for body proteins. 'Essential' amino acids can only be obtained from the food we eat as our body does not normally produce them.
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Phenylketonuria - Wikipedia, the free encyclopedia
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Phenylketonuria is an inherited disorder in which signs and symptoms vary from mild to severe. ... home > phenylketonuria index > phenylketonuria article...
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Phenylketonuria — Comprehensive overview covers symptoms, treatment (including diet information) of this rare birth defect. ... Babies in the United States and many other countries are screened for phenylketonuria soon after birth. Although phenylketonuria is rare, recognizing phenylketonuria right away can help...
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Phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. Loss of this enzyme results in mental retardation, organ damage, unusual posture and can, in cases of maternal PKU, severely compromise pregnancy.
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The National PKU News web site provides news and information about phenylketonuria, a rare, inherited metabolic disease. Web site sections include: About PKU, PKU Support Information, Diet-Related information, PKU Research, and PKU Legislation and Policy ... Before you consider trying the new PKU drug, ... Si vous parlez français,
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