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  2. Tetrahydrobiopterin deficiency - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrobiopterin_deficiency

    Tetrahydrobiopterin deficiency (THBD, BH 4 D) is a rare metabolic disorder that increases the blood levels of phenylalanine.Phenylalanine is an amino acid obtained normally through the diet, but can be harmful if excess levels build up, causing intellectual disability and other serious health problems.

  3. Dihydropteridine reductase deficiency - Wikipedia

    en.wikipedia.org/wiki/Dihydropteridine_reductase...

    Dihydropteridine reductase deficiency (DHPRD) is a genetic disorder affecting the tetrahydrobiopterin (BH4) synthesis pathway, inherited in the autosomal recessive pattern. It is one of the six known disorders causing tetrahydrobiopterin deficiency , and occurs in patients with mutations of the QDPR gene.

  4. Hyperphenylalaninemia - Wikipedia

    en.wikipedia.org/wiki/Hyperphenylalaninemia

    Phenylketonuria (PKU)-like symptoms, including more pronounced developmental defects, skin irritation, and vomiting, may appear when phenylalanine levels are near 20 mg/dL (1200 mol/L). [1] Hyperphenylalaninemia is a recessive hereditary metabolic disorder that is caused by the body's failure to convert phenylalanine to tyrosine as a result of ...

  5. Tetrahydrobiopterin - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrobiopterin

    Tetrahydrobiopterin (BH 4, THB), also known as sapropterin (), [5] [6] is a cofactor of the three aromatic amino acid hydroxylase enzymes, [7] used in the degradation of amino acid phenylalanine and in the biosynthesis of the neurotransmitters serotonin (5-hydroxytryptamine, 5-HT), melatonin, dopamine, norepinephrine (noradrenaline), epinephrine (adrenaline), and is a cofactor for the ...

  6. Pterin-4 alpha-carbinolamine dehydratase deficiency (PCDD) is one of the known forms of tetrahydrobiopterin deficiency. This condition is associated with mutations of the PCBD1 gene. As of 2020, PCDD was the rarest form of BH4 deficiency in terms of cases described in medical literature.

  7. QDPR - Wikipedia

    en.wikipedia.org/wiki/QDPR

    110391 Ensembl ENSG00000151552 ENSMUSG00000015806 UniProt P09417 Q8BVI4 RefSeq (mRNA) NM_000320 NM_001306140 NM_024236 RefSeq (protein) NP_000311 NP_001293069 NP_077198 Location (UCSC) Chr 4: 17.46 – 17.51 Mb Chr 5: 45.59 – 45.61 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse QDPR (quinoid dihydropteridine reductase) is a human gene that produces the enzyme quinoid ...

  8. How to recognize the signs and symptoms of vitamin B12 ... - AOL

    www.aol.com/news/recognize-signs-symptoms...

    Vitamin B12 deficiency causes symptoms like fatigue, poor memory, a swollen tongue, and canker sores. Skip to main content. 24/7 Help. For premium support please call: 800-290-4726 more ways to ...

  9. 6-Pyruvoyltetrahydropterin synthase deficiency - Wikipedia

    en.wikipedia.org/wiki/6-Pyruvoyltetrahydropterin...

    This is the reason that PKU and PTPS deficiency share some similar symptoms. However, since BH 4 is needed for much more than just the metabolism of Phenylalanine, there are other symptoms as well. [7] This image depicts the pathway for the synthesis if tetrahydrobiopterin, a very important cofactor in the human body.