Literature DB >> 1289568

The screening diagnosis of tetrahydrobiopterin deficient phenylketonuria.

C Ning1, S R Liu, H Wei, S Wang, D Shu, N Blau, M T Wang.   

Abstract

Since 1990, 20 diagnostically confirmed phenylketonuria (PKU) patients have been screened with a tetrahydrobiopterin (BH4) loading test, in which plasma phenylalanine and urinary pterin metabolites were investigated, ind activity of dihydropteridine reductase (DHPR) was determined as well. The results showed that there was no statistical difference between the concentrations of plasma phenylalanine before and after BH4 (20mg/kg) administration in all patients, and values of urinary neopterin and biopterin were within the range of classic PKU. All patients but one had normal activity of DHPR in red cells. This suggests that incidence of BH4 deficiency in PKU patients amounts to five percent (1/20) which is almost the same as reported abroad.

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Year:  1992        PMID: 1289568     DOI: 10.1007/bf02887852

Source DB:  PubMed          Journal:  J Tongji Med Univ        ISSN: 0257-716X


  4 in total

Review 1.  Inborn errors of pterin metabolism.

Authors:  N Blau
Journal:  Annu Rev Nutr       Date:  1988       Impact factor: 11.848

2.  [Development of the biosynthesis and excretion of pterins in phenylketonuria and its variants].

Authors:  H C Curtius; A Niederwieser
Journal:  Arch Fr Pediatr       Date:  1983

Review 3.  Tetrahydrobiopterin biosynthetic pathway and deficiency.

Authors:  A Niederwieser; H C Curtius
Journal:  Enzyme       Date:  1987

4.  Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots.

Authors:  N Arai; K Narisawa; H Hayakawa; K Tada
Journal:  Pediatrics       Date:  1982-09       Impact factor: 7.124

  4 in total

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