Birth defects occur when a baby is developing in the mother's body, usually during the first 3 months of pregnancy.
Most couples have to wait until the second trimester of
pregnancy (4-6 months), but the simple test could cut that time in half—as
early as seven weeks. The test is highly accurate, too. Of the 201 women who
were tested between 2003 and 2009, researchers were able to obtain sufficient
samples from 189 and produce 100 percent accurate results.
When a woman is pregnant, her body will circulate her blood
with blood from the fetus. For this test, a sample of the mother’s blood is
screened for genes unique to the Y-chromosome of males. If these genes were
present, researchers predicted a boy.
Early testing can also help doctors detect conditions such
as Down’s syndrome and Rhesus-D disease (RhD). This method of testing has
several advantages over invasive methods, such as fetal blood sampling (FBS),
that can cause amniotic fluid leaking or miscarriage.
RhD sometimes results from a blood incompatibility between,
for example, an Rh-positive mother and an Rh-negative child. If the mother’s
body detects this difference, it may send antibodies against the baby. If it
goes untreated, it can lead to jaundice, anemia, brain damage or stillbirth.
“Noninvasive
prenatal diagnosis of fetal Rhesus D genotype is sensitive and accurate and has
been widely validated in Europe,” authors noted. “The United States should
begin to undertake clinical trials to bring this technology to patient care as
soon as possible.”
This test is currently not available to the general public, but
continued success could mean it’s on the horizon. Its adoption into general
health practices could help cut the risk of fetal complications of RhD.
The study was published in Obstetrics&Gynecology.
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