The use of cffDNA in fetal sex determination during the first trimester of pregnancy of female DMD carriers

Intractable Rare Dis Res. 2012 Nov;1(4):157-60. doi: 10.5582/irdr.2012.v1.4.157.

Abstract

Chorionic villus sampling (CVS) or amniocentesis for fetal sex determination is generally the first step in the prenatal diagnosis of X-linked genetic disorders such as Duchenne muscular dystrophy (DMD). However, non-invasive prenatal diagnostic (NIPD) techniques such as measurement of cell-free fetal DNA (cffDNA) in maternal plasma are preferable given the procedure-related miscarriage rate of CVS. We determined fetal sex during the first trimester using a quantitative real-time polymerase chain reaction (PCR) assay of cffDNA in pregnant carriers of DMD. The fetal sex was confirmed by amniocentesis karyotype analysis and multiplex ligation-dependent probe amplification (MLPA) at 16 weeks. This procedure may avoid unnecessary CVS or amniocentesis of female fetuses.

Keywords: Cell-free fetal DNA (cffDNA); Duchenne muscular dystrophy (DMD); fetal sex determination; non-invasive prenatal diagnostic (NIPD).