Literature DB >> 1843186

Heterozygous carriers of classical phenylketonuria in a sample of the Turkish population: detection by a spectrofluorimetric method.

F Güneral1, I Ozalp, H Tatlidil.   

Abstract

Blood obtained by finger prick from 209 presumed normal homozygotes and 42 heterozygotes for classical PKU was analyzed for plasma phenylalanine (Phe) and tyrosine (Tyr) by a fluorimetric method. Subjects were tested near midday and 3 hours after a protein-rich breakfast. The plot of Phe/Tyr (micromolar ratio) against Phe2/Tyr, permitted the detection of 11 heterozygotes among 209 controls. The accuracy of this method was checked by computation of a stepwise multivariate discriminant analysis, using Phe and Tyr (mumol/L), Phe/Tyr micromolar ratio and Phe2/Tyr as variables. Ten of the 11 subjects were recovered with a percentage of correct classification of over 90%, while one case had a percentage of 89.45%. The PKU gene frequency was found to be 1/19. This emphasizes the importance of a screening programme for PKU gene carrier status in Turkey.

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Year:  1991        PMID: 1843186     DOI: 10.1007/bf01799943

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


  22 in total

1.  Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.

Authors:  K W DRISCOLL; D Y HSIA; W E KNOX; W TROLL
Journal:  Nature       Date:  1956-12-01       Impact factor: 49.962

2.  The chemical estimation of tyrosine and tyramine.

Authors:  S UDENFRIEND; J R COOPER
Journal:  J Biol Chem       Date:  1952-05       Impact factor: 5.157

3.  Inherited metabolic disorders in Turkey.

Authors:  I Ozalp; T Coskun; S Tokol; G Demircin; E Mönch
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

4.  Detection of heterozygotes for phenylketonuria by column chromatography and discriminatory analysis.

Authors:  S Rampini; P W Anders; H C Curtius; T Marthaler
Journal:  Pediatr Res       Date:  1969-07       Impact factor: 3.756

Review 5.  The phenylalanine hydroxylating system from mammalian liver.

Authors:  S Kaufman
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1971

6.  Classic phenylketonuria: diagnosis through heterozygote detection.

Authors:  R F Griffin; L J Elsas
Journal:  J Pediatr       Date:  1975-04       Impact factor: 4.406

7.  A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria.

Authors:  M A Hilton; J N Sharpe; L G Hicks; B F Andrews
Journal:  J Pediatr       Date:  1986-10       Impact factor: 4.406

Review 8.  Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Authors:  F Güttler
Journal:  Acta Paediatr Scand Suppl       Date:  1980

9.  Serum tyrosine within the first hour after an oral load of phenylalanine.

Authors:  F Güttler; G Hansen
Journal:  Scand J Clin Lab Invest       Date:  1977-12       Impact factor: 1.713

10.  Carrier screening for phenylketonuria: comparison of two discriminant analysis procedures.

Authors:  C L Freehauf; D Lezotte; S I Goodman; E R McCabe
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

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  1 in total

1.  Elevated plasma phenylalanine in severe malaria and implications for pathophysiology of neurological complications.

Authors:  Bert K Lopansri; Nicholas M Anstey; Gregory J Stoddard; Esther D Mwaikambo; Craig S Boutlis; Emiliana Tjitra; Helena Maniboey; Maurine R Hobbs; Marc C Levesque; J Brice Weinberg; Donald L Granger
Journal:  Infect Immun       Date:  2006-06       Impact factor: 3.441

  1 in total

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