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. 1973 Jun;10(2):120–121. doi: 10.1136/jmg.10.2.120

Tissue Culture Techniques as an Aid to Prenatal Diagnosis and Genetic Counselling in Homocystinuria

A H Bittles 1, Nina A J Carson 1
PMCID: PMC1012999  PMID: 4714577

Abstract

Cystathionine synthase activity was studied in skin fibroblasts from a mother with homocystinuria and her husband and newborn baby. Enzyme studies were also undertaken on a fibroblast cell line derived from amniotic fluid taken at 16 weeks' gestation. The enzyme activity was very low in the mother, within the normal range in the father, and at an intermediate level consistent with heterozygosity in the infant. The activity present in the amnion fibroblasts was similar to that found in the cell line cultured from the infant's skin biopsy.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. CARSON N. A., NEILL D. W. Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland. Arch Dis Child. 1962 Oct;37:505–513. doi: 10.1136/adc.37.195.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. FINKELSTEIN J. D., MUDD S. H., IRREVERRE F., LASTER L. HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE. Science. 1964 Nov 6;146(3645):785–787. doi: 10.1126/science.146.3645.785. [DOI] [PubMed] [Google Scholar]
  3. GERRITSEN T., VAUGHN J. G., WAISMAN H. A. The identification of homocystine in the urine. Biochem Biophys Res Commun. 1962 Dec 19;9:493–496. doi: 10.1016/0006-291x(62)90114-6. [DOI] [PubMed] [Google Scholar]
  4. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  5. MUDD S. H., FINKELSTEIN J. D., IRREVERRE F., LASTER L. HOMOCYSTINURIA: AN ENZYMATIC DEFECT. Science. 1964 Mar 27;143(3613):1443–1445. doi: 10.1126/science.143.3613.1443. [DOI] [PubMed] [Google Scholar]
  6. Mudd S. H., Finkelstein J. D., Irreverre F., Laster L. Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway. J Biol Chem. 1965 Nov;240(11):4382–4392. [PubMed] [Google Scholar]
  7. Seashore M. R., Durant J. L., Rosenberg L. E. Studies of the mechanism of pyridoxine-responsive homocystinuria. Pediatr Res. 1972 Mar;6(3):187–196. doi: 10.1203/00006450-197203000-00007. [DOI] [PubMed] [Google Scholar]
  8. Uhlendorf B. W., Mudd S. H. Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria. Science. 1968 May 31;160(3831):1007–1009. doi: 10.1126/science.160.3831.1007. [DOI] [PubMed] [Google Scholar]

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