DNA from the fetus circulates in maternal blood. Unlike intact fetal cells in maternal blood, which can persist for years after a pregnancy, circulating cell-free fetal DNA (ccffDNA) results from the breakdown of fetal cells (mostly placental) and clears from the maternal system within hours. Fetal DNA detected during a pregnancy, therefore, represents DNA from the current fetus. Although only about 10-15% of the cell-free DNA circulating in maternal blood is from the fetus, it can be detected and measured. Quantitative differences in chromosome fragments in maternal blood can be used to distinguish fetuses affected with trisomy 21, and a few other fetal aneuplodies, from those that are not affected.
At least one laboratory will accept samples that do not meet these high risk criteria. Additionally, at least one laboratory offers the test in twin pregnancies, and another for Turner syndrome (monosomy X) when the fetus presents with a cystic hygroma. Contact individual laboratories for additional information.
Re: Genetic Testing ... are you going to do it?
DD 12/20/99, DS 12/14/12, M/C 9/2014, M/C 1/2015
\ My husband and I talked about it quite a bit - and the only way we would consider not having the baby is if it had some genetic defect where it would live a horrible life in pain for a year or a few years and then have no chance of survival. Because we don't think that brining the baby into a terrible life of pain is necessarily the right thing to do either.
NEW PEANUT DUE 7.2017
NEW PEANUT DUE 7.2017
I 100% wanted to have the cell free DNA test done. I think arming yourself with information is crucial!