Literature DB >> 1159582

Prenatal diagnosis of cystinosis.

B States, B Blazer, D Harris, S Segal.   

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 35SL-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 nonprotein-free 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.

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Year:  1975        PMID: 1159582     DOI: 10.1016/s0022-3476(75)80820-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  2 in total

1.  Infantile nephropathic cystinosis presenting as incomplete Fanconi syndrome and refractory rickets.

Authors:  V S Rajadurai; P Shanbag; M S Seshadri; U Khanduri; T A Alexander; M A Jadhav
Journal:  Indian J Pediatr       Date:  1989 May-Jun       Impact factor: 1.967

Review 2.  Cystinosis: a review.

Authors:  Mohamed A Elmonem; Koenraad R Veys; Neveen A Soliman; Maria van Dyck; Lambertus P van den Heuvel; Elena Levtchenko
Journal:  Orphanet J Rare Dis       Date:  2016-04-22       Impact factor: 4.123

  2 in total

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