Literature DB >> 20963478

Non-invasive prenatal detection of achondroplasia using circulating fetal DNA in maternal plasma.

Ji Hyae Lim1, Mee Jin Kim, Shin Young Kim, Hye Ok Kim, Mee Jin Song, Min Hyoung Kim, So Yeon Park, Jae Hyug Yang, Hyun Mee Ryu.   

Abstract

PURPOSE: To perform a reliable non-invasive detection of the fetal achondroplasia using maternal plasma.
METHODS: We developed a quantitative fluorescent-polymerase chain reaction (QF-PCR) method suitable for detection of the FGFR3 mutation (G1138A) causing achondroplasia. This method was applied in a non-invasive detection of the fetal achondroplasia using circulating fetal-DNA (cf-DNA) in maternal plasma. Maternal plasmas were obtained at 27 weeks of gestational age from women carrying an achondroplasia fetus or a normal fetus.
RESULTS: Two percent or less achondroplasia DNA was reliably detected by QF-PCR. In a woman carrying a normal fetus, analysis of cf-DNA showed only one peak of the wild-type G allele. In a woman expected an achondroplasia fetus, analysis of cf-DNA showed the two peaks of wild-type G allele and mutant-type A allele and accurately detected the fetal achondroplasia.
CONCLUSIONS: The non-invasive method using maternal plasma and QF-PCR may be useful for diagnosis of the fetal achondroplasia.

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Year:  2010        PMID: 20963478      PMCID: PMC3059531          DOI: 10.1007/s10815-010-9489-1

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  18 in total

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7.  Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin.

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