Plasma phenylalanine and tyrosine levels revisited in heterozygotes for hyperphenylalaninaemia
- 5 May 1992
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 16 (1) , 105-109
- https://doi.org/10.1007/bf00711323
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.Keywords
This publication has 21 references indexed in Scilit:
- Review of neonatal screening programme for phenylketonuria.BMJ, 1991
- Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.Journal of Medical Genetics, 1978
- Use of overlapping normal distributions in genetic counselling.Journal of Medical Genetics, 1978
- Heterozygote detection in phenylketonuriaClinical Genetics, 1977
- Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.Journal of Medical Genetics, 1975
- Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Determination of heterozygosity for phenylketonuria on the amino acid analyzerClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- A simple test for heterozygosity for phenylketonuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responsesThe Journal of Pediatrics, 1962
- Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of PhenylketonuriaNature, 1956