Prenatal diagnosis of cystinosis

dc.contributor.authorStates, Beatrice
dc.contributor.authorBlazer, Bonnie
dc.contributor.authorHarris, Dorothy
dc.contributor.authorSegal, Stanton
dc.date.accessioned2018-07-12T20:13:20Z
dc.date.available2018-07-12T20:13:20Z
dc.date.issued1975-10
dc.description.abstractCystinosis 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.citationBeatrice 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.urihttps://hdl.handle.net/1805/16664
dc.subjectCystinosisen_US
dc.subjectPrenatal Diagnosisen_US
dc.subjectCystine Crystalsen_US
dc.titlePrenatal diagnosis of cystinosisen_US
dc.typeArticleen_US
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