Literature DB >> 15539874

Prenatal diagnosis of common aneuploidies using multiplex quantitative fluorescent polymerase chain reaction.

S El Mouatassim1, M Becker, S Kuzio, C Ronsin, S Gil, M Nouchy, L Druard, F Forestier.   

Abstract

OBJECTIVE: Prenatal diagnosis of foetal trisomies is usually performed by cytogenetic analysis. This requires lengthy laboratory procedures and it is expensive. Here, we report a retrospective study of quantitative fluorescent polymerase chain reaction (QF-PCR) for prenatal detection of trisomies 13, 18 and 21.
METHODS: QF-PCR was performed on a total of 447 amniotic fluids blindly analysed without any knowledge of the cytogenetic results and 43 samples with known karyotype. All samples were tested with at least 4 small tandem repeat markers specific for each chromosome 13, 18 or 21.
RESULTS: QF-PCR results on amniotic fluid were consistent with conventional cytogenetic data. QF-PCR detected 5 cases of trisomy 21, 2 cases of trisomy 18, 1 case of trisomy 13 and 1 case with Klinefelter's syndrome.
CONCLUSIONS: QF-PCR has proved to be very useful in clinical settings, since it allows the detection of major numerical disorders in a few hours after sampling and thus reduces parental anxiety. 2004 S. Karger AG, Basel.

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Year:  2004        PMID: 15539874     DOI: 10.1159/000080162

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  2 in total

1.  Practical application of fluorescent quantitative PCR on Trisomy 21 in Chinese Han population.

Authors:  Xiaobo Sun; Ming Yan; Yuanzhen Zhang; Xin Zhou; Chunhong Wang; Fang Zheng; Chenling Xiong
Journal:  Mol Biol Rep       Date:  2006-09       Impact factor: 2.316

2.  Molecular detection of trisomy 21 by bicolor competitive fluorescent PCR.

Authors:  Yan Wang; Xiaofei Zhang; Bo Ling; Changxiao He; Qingjie Xia; Feng Chen; Isamu Miyamori; Zhao Yang; Chunyuan Fan
Journal:  J Clin Lab Anal       Date:  2013-05       Impact factor: 2.352

  2 in total

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