Abstract
A pregnancy at risk for adenosine deaminase deficiency and severe combined immunodeficiency disease was investigated using samples of chorionic villi obtained during the eighth week of pregnancy. Adenosine deaminase levels suggested that the fetus was a probable carrier and that a diagnosis of severe combined immunodeficiency disease could be excluded. Enzyme and chromosome results were available within 24 hours of the chorionic villous sampling procedure, and were confirmed on amniotic fluid cell cultures after amniocentesis at 17 weeks' gestation and on cord blood at delivery.
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Selected References
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- Hirschhorn R., Beratis N., Rosen F. S., Parkman R., Stern R., Polmar S. Adenosine-deaminase deficiency in a child diagnosed prenatally. Lancet. 1975 Jan 11;1(7898):73–75. doi: 10.1016/s0140-6736(75)91075-2. [DOI] [PubMed] [Google Scholar]
- Kleijer W. J., van Diggelen O. P., Janse H. C., Galjaard H., Dumez Y., Boué J. First trimester diagnosis of Hunter syndrome on chorionic villi. Lancet. 1984 Aug 25;2(8400):472–472. doi: 10.1016/s0140-6736(84)92952-0. [DOI] [PubMed] [Google Scholar]
- 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]
- Linch D. C., Levinsky R. J. Prenatal diagnosis of immunodeficiency disorders. Br Med Bull. 1983 Oct;39(4):399–404. doi: 10.1093/oxfordjournals.bmb.a071854. [DOI] [PubMed] [Google Scholar]
- Linch D. C., Levinsky R. J., Rodeck C. H., Maclennan K. A., Simmonds H. A. Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiency. Clin Exp Immunol. 1984 May;56(2):223–232. [PMC free article] [PubMed] [Google Scholar]
