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Phenylketonuria

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Jump to Comments From Vitasearch... by Duane Sherry, M.S., CRC ... ents with PKU Linked to Reduced Cognitive FunctionKeywords:PKU, PHENYLKETONURIA, COGNITIVE FUNCTION - Selenium, Antioxidant, Ret ...
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Aspartame Jane N. ... ALANINE on it? Some individuals are born with a disease called Phenylketonuria (PKU) where phenylalanine can’t be disposed of i ...
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... s such as those described below. Phenylketonuria (PKU) - this is an inherited condition that affe ...
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Autism and Mitochondrial Disorders by Dr. Charlotte Thompson, MD ... went on to say that other "inborn errors of metablism, such as phenylketonuria and disorders of purine metabolism, and a variet ...
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Artificial sweeteners vs Sugar by Mary Ellen B. ... . It isn’t safe for people who have the rare hereditary disease phenylketonuria (PKU). Products that contain aspartame must carr ...
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Update from our trip to UCLA! by Kelly ... ave ruled out some other possible genetic causes including PKU (Phenylketonuria), SCAD (short chain acyl-coa Dehydrogenase Defic ...
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Info on aspartame from the ADA Lisa T. ... ritional needs. Individuals with the rare genetic disease, phenylketonuria (PKU), cannot properly metabolize phenylalanine. ...
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phenylketonuria trusted sourcesTrusted Web Resources

 
Phenylketonuria - Wikipedia, the free encyclopedia
Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the enzyme phenylalanine hydroxylase (PAH). ...

MedlinePlus: Phenylketonuria
The primary NIH organization for research on Phenylketonuria is the National ... Phenylketonuria (PKU) is a genetic disorder in which the body can't process ...

Phenylketonuria
PHENYLKETONURIA (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. Loss of this enzyme results in ...

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. ...

MedlinePlus Medical Encyclopedia: Phenylketonuria
Phenylketonuria (PKU) is a rare condition in which a baby is born ... Phenylketonuria (PKU) is inherited, which means it is passed down through families. ...

OMIM - PHENYLKETONURIA
MIM +261600 · Description · Clinical Features · Biochemical Features · Inheritance · Mapping · Molecular Genetics · Genotype/Phenotype Correlations ...

PKU (Phenylketonuria) - March of Dimes
PKU (phenylketonuria) is an inherited disorder that can cause mental retardation . With newborn screening, almost all affected newborns are diagnosed and ...

Phenylketonuria
Phenylketonuria Phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. ...

phenylketonuria newsNews

 
BioMarin's partner Merck wins EU positive opinion for ...
We are excited to work with our partner Merck Serono to offer the first therapeutic option to manage phenylketonuria in the European market. ...

EU drugs agency recommends approval of Kuvan
The London-based watchdog said Kuvan was recommended for the treatment of hyperphenylalaninaemia in patients with phenylketonuria. ...

Merck Serono’s Kuvan Recommended for European Approval
... for Merck Serono’s Kuvan as an oral treatment for hyperphenylalaninemia in patients with phenylketonuria (PKU) or tetrahydrobiopterin (BH4) deficiency. ...

Merck KGaA’s Kuvan Recommended for European Approval
1Kuvan® is indicated for “the treatment of hyperphenylalaninaemia (HPA) in adult and paediatric patients of 4 years of age and over with phenylketonuria ...

phenylketonuria web resultsWeb Results

 
Phenylketonuria
Answers to your questions about phenylketonuria and more! Information you can trust: patient guides, the latest news, tips, tools, animations and ...

IBEX TECHNOLOGIES GAINS U.S. ORPHAN DRUG DESIGNATION FOR PHENYLASE ...
PKU - Phenylketonuria A genetic disorder in which the body lacks the enzyme necessary to metabolize phenylalanine to tyrosine. Left untreated, the disorder ...

Sugar Substitutes and artificial sweeteners information from ...
People with advanced liver disease, women with certain genetic traits (i.e., phenylketonuria), and pregnant women with high levels of phenylalanine in the ...

Glyko Biomedical Ltd.'s 27%-owned Affiliate, BioMarin To Acquire ...
In addition, IBEX has an early development stage program for Phenylase, an orally active enzyme with the potential to treat Phenylketonuria (PKU), ...

Ph-Pk
Phenylketonuria: Also Known As: "PKU" A genetic disorder in which the enzyme that metabolizes the amino acid phenylalanine is lacking. ...

Eastern Biotech Offers Premarital Screening in Middle East. - Free ...
Uridyltransferase, Phenylketonuria, Organic Acidemias, Acylcarnitine Profile ... Phenylketonuria Organic Acidemias: - 3 Hydroxy 3 Methylglutaryl CoA Lyase ...

Newborn Care Health Center
Additional issues include fetal alcohol syndrome, phenylketonuria or pyloric stenosis. More common but less serious issues include thrush, colic, ...

Aspartame: Is aspartame safe during pregnancy?
One is PKU, or phenylketonuria. This is an inborn error of metabolism, where a person cannot properly metabolize phenylalanine. I don't believe this is an ...

phenylketonuria blogsBlog Articles

 
Phenylketonuria
Besides the mental deterioration and their peculiar odour, children with phenylketonuria can be recognised by their tendency to fair hair and pale colouration of the skin. Genetic studies showed that the condition is attributable to a ...

Maternal Phenylketonuria
Women of childbearing age with all forms of phenylketonuria, including mild variants such as mild hyperphenylalaninemia, should receive counseling concerning their risks for adverse fetal effects, optimally before conceiving. ...

what does phenylketonuria mean?
... to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency Synonym(s) PKU (what does PKU mean?) Hypernyms(s) phenylketonuria is a kind of… ...

phenylketonuria questions & answersQuestions & Answers

 
 

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