Literature DB >> 8487490

Plasma phenylalanine and tyrosine levels revisited in heterozygotes for hyperphenylalaninaemia.

J M Saraiva1, J W Seakins, I Smith.   

Abstract

We examined the value of the fasting plasma phenylalanine/tyrosine ratio obtained in an ordinary clinical setting for assessing the probability of being a heterozygote for hyperphenylalaninaemia. This biochemical test was found to be of little value in those with a high (66%) prior risk of heterozygosity, because it could not reduce the risk below 12%. However, in a population with a prior risk of only 2%, it discriminates the 3% with a 19% risk from the 97% with a risk of 1.5% or less. This simple method could usefully be applied to such a population, in order to select those at higher risk for further investigation using molecular genetics.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8487490     DOI: 10.1007/bf00711323

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  19 in total

1.  Increased reliability for the determination of the carrier state in phenylketonuria.

Authors:  H L WANG; N E MORTON; H A WAISMAN
Journal:  Am J Hum Genet       Date:  1961-06       Impact factor: 11.025

2.  Phenylketonuria: a linkage study using phenylalanine tolerance tests.

Authors:  J H RENWICK; S D LAWLER; V A COWIE
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

3.  Amino acid analysis of physiological fluids by high-performance liquid chromatography with phenylisothiocyanate derivatization and comparison with ion-exchange chromatography.

Authors:  J F Davey; R S Ersser
Journal:  J Chromatogr       Date:  1990-06-08

4.  Effects of oral contraceptives and obesity on carrier tests for phenylketonuria.

Authors:  E S Brown; H A Waisman; M A Swanson; R E Colwell; M E Banks; T Gerritsen
Journal:  Clin Chim Acta       Date:  1973-03-14       Impact factor: 3.786

5.  Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.

Authors:  K Blau; G K Summer; H C Newsome; C H Edwards
Journal:  Clin Chim Acta       Date:  1973-05-18       Impact factor: 3.786

6.  Detection of phenylketonuric heterozygotes.

Authors:  S H Jackson; W B Hanley; T Gero; G D Gosse
Journal:  Clin Chem       Date:  1971-06       Impact factor: 8.327

7.  Heterogeneity in genetic control of phenylalanine metabolism in man.

Authors:  D Rosenblatt; C R Scriver
Journal:  Nature       Date:  1968-05-18       Impact factor: 49.962

Review 8.  The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.

Authors:  D S Konecki; U Lichter-Konecki
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

9.  Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.

Authors:  S Bundey
Journal:  J Med Genet       Date:  1978-08       Impact factor: 6.318

10.  Use of overlapping normal distributions in genetic counselling.

Authors:  N R Dennis; C O Carter
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

View more
  2 in total

Review 1.  Dopa-responsive dystonia, DRD-plus and DRD look-alike: a pragmatic review.

Authors:  Ajith Cherian; Naveen Kumar Paramasivan; K P Divya
Journal:  Acta Neurol Belg       Date:  2021-01-16       Impact factor: 2.396

Review 2.  Clinical spectrum of dopa-responsive dystonia and related disorders.

Authors:  Woong-Woo Lee; Beom Seok Jeon
Journal:  Curr Neurol Neurosci Rep       Date:  2014-07       Impact factor: 5.081

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.