Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/133669
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dc.titleRapid karyotyping of spontaneous abortions with trophoblastic villi.
dc.contributor.authorChua, S.
dc.contributor.authorYeoh, S.C.
dc.contributor.authorNg, P.L.
dc.contributor.authorHagarty, A.
dc.contributor.authorRauff, M.
dc.contributor.authorRatnam, S.S.
dc.date.accessioned2016-12-20T08:38:43Z
dc.date.available2016-12-20T08:38:43Z
dc.date.issued1989-01
dc.identifier.citationChua, S., Yeoh, S.C., Ng, P.L., Hagarty, A., Rauff, M., Ratnam, S.S. (1989-01). Rapid karyotyping of spontaneous abortions with trophoblastic villi.. Annals of the Academy of Medicine Singapore 18 (1) : 52-54. ScholarBank@NUS Repository.
dc.identifier.issn03044602
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/133669
dc.description.abstract24-hour short term culture of trophoblastic villi provided rapid and accurate karyotypes in spontaneous first trimester abortions. Good quality metaphases were obtained in 60.0% of villous cultures if these were set up within 8 hours of uterine evacuation, in contrast to the 10.3% success rate with intervals longer than 8 hours. 21% (4 of 19) of first trimester pregnancy losses were chromosomally abnormal, 3 of which were examples of autosomal trisomy; in 2 cases, the mothers were more than 37 years of age. The results of successful karyotyping reported here compare well with previous reports of long term culture of minced fetal material. Further, the risks of infected cultures, maternal contamination and pseudomosaicism are minimal with the short-term culture technique described here. Chorionic villi isolated from spontaneously aborted material are a simple and practicable source of fetal material for rapid and accurate cytogenic diagnosis in early spontaneous abortions.
dc.typeArticle
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.description.sourcetitleAnnals of the Academy of Medicine Singapore
dc.description.volume18
dc.description.issue1
dc.description.page52-54
dc.identifier.isiutNOT_IN_WOS
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