Detection of heterozygotes for homocystinuria: Study of sulphur-containing amino acids in plasma and urine after L-methionine loading
I. B. Sardharwalla, Brian Fowler, A. J. Robins, G. M. Komrower
Abstract
I. B. Sardharwalla, Brian Fowler, A. J. Robins, G. M. Komrower
Abstract
Twelve parents of patients with homocystinuria and 12 normal control subjects were given standard L-methionine loads. Determination of plasma concentrations of homocystine and cysteine-homocysteine disulphide, of urine concentration ratios of homocystine: cystine, cysteine-homocysteine disulphide: cystine, and homocysteic acid: cysteic acid allowed a distinction to be made between the two groups. The findings indicate the value of the L-methionine loading test for detection of heterozygotes for homocystinuria, particularly where facilities for fibroblast culture and cystathionine synthase assay are not available.
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Twelve parents of patients with homocystinuria and 12 normal control subjects were given standard L-methionine loads. Determination of plasma concentrations of homocystine and cysteine-homocysteine disulphide, of urine concentration ratios of homocystine: cystine, cysteine-homocysteine disulphide: cystine, and homocysteic acid: cysteic acid allowed a distinction to be made between the two groups. The findings indicate the value of the L-methionine loading test for detection of heterozygotes for homocystinuria, particularly where facilities for fibroblast culture and cystathionine synthase assay are not available.
Key concepts: Homocystinuria, Cystine, Cystathionine beta synthase, Methionine, Cysteic acid, Homocysteine, Cystinuria, Cysteine