«We may be able to use it to
detect sickle cells.»
Not exact matches
As early as the first trimester, doctors can take a sample of placental tissue (chorionic villus sampling, or CVS) to
detect whether a baby has the genes that would lead to
sickle cell anemia or
sickle cell trait.
Some other abnormalities that can be
detected from these special tests include Down Syndrome, Turners» Syndrome, Tay - Sachs disease,
sickle cell anemia, Edwards Syndrome.
Over the next few years, similar maternal blood tests could
detect hundreds of diseases caused by chromosome abnormalities or mutations, including cystic fibrosis,
sickle cell anemia, Tay - Sachs disease, and genetic deafness and blindness.
Despite universal newborn screening that
detects the presence of
sickle cell trait (SCT), only 16 percent of Americans with SCT know their status.