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Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the enzyme hepatic phenylalanine hydroxylase. :541 This enzyme is necessary to metabolize the amino acid phenylalanine to the...
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Online resource that offers Phenylketonuria (PKU) related information, facts, news, personal stories, and discussion forum.
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Information for families and health care professionals interested in Phenylketonuria (PKU)
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PKU (phenylketonuria), in its "classic" form, is a rare, inherited metabolic ... The diet for PKU was developed in the 1960's, and until December 2007 when the ...
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PKU (phenylketonuria) is an inherited disorder that can cause mental retardation. ... At least 1 baby in 25,000 is born with PKU in the United States (1) ...
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Welcome to the March of Dimes ... in 25,000 is born with PKU in the United States (1) ... Children with untreated PKU often are irritable and have ...
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Definition, causes, symptoms ... Phenylketonuria (PKU) is a genetic disorder that is ... In classic PKU, levels may range from 6 to 80mg/dl, but are ...
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The Case of PKU Dietary Coverage. Dietary Specialties - Low Protein Foods ... Mid-Atlantic Connection for PKU and Allied Disorders ...
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In PKU, the body can't process a portion of the protein called phenylalanine ... The most effective treatment for PKU is a special diet of foods that help ...
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Can other members of the family have PKU or be carriers? Can other family members be tested? ... Does PKU go by any other names? Where can I find more information? ...
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Home Page for the National PKU Alliance for advocacy and support of families with phenylketonuria. ... PKU Information Kit. Press. Donate. Conference ...
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Phenylketonuria ... Treatment of Phenylketonuria (PKU)(Food and Drug ... Article: Adults with late diagnosed PKU and severe challenging behaviour. ...
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Definition, causes, symptoms and treatment. ... Babies with PKU are missing an enzyme called phenylalanine hydroxylase, which is ... PKU is a treatable disease. ...
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Phenylketonuria (PKU) is a genetic condition associated with abnormally high ... In order to understand PKU, it is necessary to understand some basic concepts of ...
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More about Phenylketonuria: Causes and symptoms Diagnosis Treatment Resources Phenylketonuria Definition Phenylketonuria (PKU) is a rare, inherited,
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Read an article that explains a serious life-long disease that can be diagnosed at birth and treated to prevent brain damage.
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Presentation of the institutes and departments, international admission and exchange programs, and a picture gallery.
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Phenylketonuria (fennel-key-ton-uria) is often called PKU for short. ... At the present time, a diet low in "phe" is the only treatment for PKU. ...
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Phenylketonuria (PKU) is an autosomal recessive genetic disorder caused by a ... In a child with PKU there is no chemical reaction to convert phenylalanine to ...
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Phenylketonuria (PKU), an inherited disorderis an inherited disorder in which ... If PKU is not treated, phenylalanine can build up to harmful levels in the body, ...
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