Tetrahydrobiopterin deficiency

Results: 11



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1Coenzymes / Pteridines / Alcohols / Lactams / Tetrahydrobiopterin / Phenylketonuria / 6-Pyruvoyltetrahydropterin synthase deficiency / Phenylalanine hydroxylase / Pharmaceutical Benefits Scheme / Medicine / Health / Chemistry

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Source URL: www.pbs.gov.au

Language: English - Date: 2014-10-01 21:56:22
2Mental retardation / Phenylketonuria / PKU / Phenylalanine / Dominance / Hyperphenylalanemia / Medical genetics / Newborn screening / Tetrahydrobiopterin deficiency / Medicine / Health / Biology

Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called

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Source URL: health.state.tn.us

Language: English - Date: 2007-05-01 15:48:27
3Medicine / Biology / Pediatrics / PKU / Phenylalanine / Newborn screening / Dominance / Tetrahydrobiopterin deficiency / Hyperphenylalanemia / Health / Mental retardation / Phenylketonuria

Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a

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Source URL: www.maine.gov

Language: English - Date: 2011-11-10 05:39:05
4Mental retardation / Phenylketonuria / Coenzymes / Pteridines / Tetrahydrobiopterin / PKU / Medical genetics / Phenylalanine hydroxylase / Phenylalanine / Medicine / Health / Chemistry

Phenylketonuria (PKU) (metabolic condition: amino acid disorder) Also known as: • phenylalanine hydroxylase deficiency

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Source URL: www.albertahealthservices.ca

Language: English - Date: 2013-09-16 18:35:23
5

Diagnosis: Tetrahydrobiopterin Deficiency (BH4) Diagnosis: Tetrahydrobiopterin Deficiency (BH4) BH4 is an inherited disorder that increases the blood levels off phenylalanine, an amino acid obtained through the diet. It

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Source URL: www.wadsworth.org

- Date: 2009-07-15 13:48:22
    6Mental retardation / Phenylketonuria / PKU / Phenylalanine / Dominance / Hyperphenylalanemia / Medical genetics / Newborn screening / Tetrahydrobiopterin deficiency / Medicine / Health / Biology

    Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called

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    Source URL: health.tn.gov

    Language: English - Date: 2007-05-01 15:48:27
    7Pteridines / Organic chemistry / Mental retardation / Phenylketonuria / Tetrahydrobiopterin / PKU / Biopterin / Phenylalanine / Disease / Chemistry / Health / Coenzymes

    Climb National Information Centre for Metabolic Diseases Tetrahydrobiopterin Deficiency - General • •

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    Source URL: www.climb.org.uk

    Language: English - Date: 2014-03-19 09:33:49
    8Medicine / Genetic genealogy / Newborn screening / PKU / Phenylalanine / Hyperphenylalanemia / Tetrahydrobiopterin deficiency / Health / Mental retardation / Phenylketonuria

    Parent Fact Sheet Phenylketonuria (PKU) (Fee nul key tone your ee a) What is PKU? Phenylketonuria (PKU) is a metabolic disorder. This means the body has a chemical imbalance. PKU is

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    Source URL: www.vdh.virginia.gov

    Language: English - Date: 2014-04-08 11:13:09
    9Mental retardation / Phenylketonuria / PKU / Phenylalanine / Dominance / Hyperphenylalanemia / Medical genetics / Newborn screening / Tetrahydrobiopterin deficiency / Medicine / Health / Biology

    Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called

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    Source URL: health.state.tn.us

    Language: English - Date: 2007-05-01 15:48:27
    10Tetrahydrobiopterin deficiency / Phenylketonuria / Phenylalanine hydroxylase / Tetrahydrobiopterin / Phenylalanine / PKU / Medical genetics / Newborn screening / Neurotransmitter / Medicine / Health / Chemistry

    Visio-Phenylalanine[removed] no edits.vsd

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    Source URL: www.ncbi.nlm.nih.gov

    Language: English
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