Prenatal diagnosis of cystinosis
dc.contributor.author | States, Beatrice | |
dc.contributor.author | Blazer, Bonnie | |
dc.contributor.author | Harris, Dorothy | |
dc.contributor.author | Segal, Stanton | |
dc.date.accessioned | 2018-07-12T20:13:20Z | |
dc.date.available | 2018-07-12T20:13:20Z | |
dc.date.issued | 1975-10 | |
dc.description.abstract | Cystinosis was diagnosed in a small quantity of cultured amniotic cells from a 22-week-old fetus by a modified pulse-labeling technique in which intracellular 55Sl-cystine retention was measured. As a result of the above finding, the pregnancy was terminated by administration of prostaglandin. The diagnosis was confirmed when the nonprotien-free cystine cystine content of the kidney, liver, placenta, spleen, thymus, and gut, as well as that of a large amount of cultured amniotic cells, was found to be 100-fold higher than normal levels. | en_US |
dc.identifier.citation | Beatrice States, Ph.D, Bonnie Blazer, B.A., Dorothy Harris, and Stanton Segal, M.D. Prenatal diagnosis of cystinosis. The Journal of Pediatrics. October 1975. | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/16664 | |
dc.subject | Cystinosis | en_US |
dc.subject | Prenatal Diagnosis | en_US |
dc.subject | Cystine Crystals | en_US |
dc.title | Prenatal diagnosis of cystinosis | en_US |
dc.type | Article | en_US |