Standardized loading test with protein for the differentiation of phenylketonuria from hyperphenylalaninaemia
- 1 March 1982
- journal article
- research article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 5 (1) , 29-35
- https://doi.org/10.1007/bf01799751
Abstract
Eighty-nine protein-loading tests were performed in 80 patients with an increased blood phenylalanine concentration. The amount of protein corresponding to 0.18g phenylalanine/kg body weight per day was calculated and given for 3 days, during which time eight phenylalanine and eight tyrosine blood concentrations were determined. Nine numerical evaluations were checked for discrimination between phenylketonuria and hyperphenylalaninaemia. The two most powerful discriminants were the phenylalanine blood concentration after 72 hours (sample taken in the morning of the 4th day after the beginning of the load) with a limit value of 15 mg/dl (0.91 mmol/l), and the mean value of the 5th to 8th phenylalanine values, also with a limit value of 15 mg/dl. In only eight of the 80 patients would the final diagnosis not have been established by the loading test.This publication has 19 references indexed in Scilit:
- Sensitive in vivo assay of the phenylalanine hydroxylating system with a small intravenous dose of heptadeutero l-phenylalanine using high pressure liquid chromatography and capillary gas chromatography/mass fragmentographyClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterinClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- ON INDICATIONS FOR TREATMENT OF THE HYPERPHENYLALANINEMIC NEONATEActa Paediatrica, 1977
- Determination of deuterium-labeled phenylalanine and tyrosine in human plasma with high pressure liquid chromatography and mass spectrometryClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Phenylketonuria variantsPublished by Springer Nature ,1976
- Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and HyperphenylalaninemiaPediatric Research, 1975
- Letter: Phenylalaninaemia.Archives of Disease in Childhood, 1975
- Phenylalaninaemia: Differential diagnosisArchives of Disease in Childhood, 1974
- Phenylalanine hydroxylase of human liver: Assay and some propertiesArchives of Biochemistry and Biophysics, 1969
- Detection of Heterozygotes for Phenylketonuria by Column Chromatography and Discriminatory AnalysisPediatric Research, 1969