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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1977 Apr;14(2):100–102. doi: 10.1136/jmg.14.2.100

Rapid prenatal diagnosis of the Lesch-Nyhan syndrome.

D Halley, M J Heukels-Dully
PMCID: PMC1013522  PMID: 856956

Abstract

Autoradiographic demonstration of 3H-hypoxanthine incorporation in small numbers of amniotic fluid cells cultured on coverslips is a rapid and practical technique in the prenatal diagnosis of the Lesch-Nyhan mutation. An affected male fetus, a normal male fetus, and a heterozygous female fetus were identified within 14 days after amniocentesis in three pregancies at risk for the Lesch-Nyhan syndrome.

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Selected References

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  1. Boyle J. A., Raivio K. O., Astrin K. H., Schulman J. D., Graf M. L., Seegmiller J. E., Jacobsen C. B. Lesch-Nyhan syndrome: preventive control by prenatal diagnosis. Science. 1970 Aug 14;169(3946):688–689. doi: 10.1126/science.169.3946.688. [DOI] [PubMed] [Google Scholar]
  2. Fujimoto W. Y., Seegmiller J. E., Uhlendorf B. W., Jacobson C. B. Biochemical diagnosis of an X-linked disease in utero. Lancet. 1968 Aug 31;2(7566):511–512. doi: 10.1016/s0140-6736(68)90671-5. [DOI] [PubMed] [Google Scholar]
  3. Niermeijer M. F., Halley D., Sachs E., Tichelaar-Klepper C., Garver K. L. Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases. Humangenetik. 1973;20(2):175–178. doi: 10.1007/BF00284856. [DOI] [PubMed] [Google Scholar]
  4. Richardson B. J., Cox D. M. Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and Tay-Sachs patients and amniotic fluid cells. Clin Genet. 1973;4(5):376–380. doi: 10.1111/j.1399-0004.1973.tb01163.x. [DOI] [PubMed] [Google Scholar]
  5. Van Heeswijk P. J., Blank C. H., Seegmiller J. E., Jacobson C. B. Preventive control of the Lesch-Nyhan syndrome. Obstet Gynecol. 1972 Jul;40(1):109–113. [PubMed] [Google Scholar]
  6. Willers I., Agarwal D. P., Singh S., Schloot W., Goedde H. W. Rapid determination of hypoxanthine-guanine-phosphoribosyl transferase in human fibroblasts and amniotic cells. Humangenetik. 1975;27(4):323–328. doi: 10.1007/BF00278425. [DOI] [PubMed] [Google Scholar]

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