| Our Prenatal Diagnosis Services |
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Ultrasound – the
painless use of sound waves to create detailed
moving pictures of your baby in real-time,
allowing our sonologists to evaluate fetal
growth and to detect fetal malformations.
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Amniocentesis – the
removal (under continuous ultrasound guidance)
of a small amount of fluid surrounding the baby,
which can be used to detect chromosomal problems,
open neural tube defects and
other inherited conditions, and to determine
fetal
lung maturity. |
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Chorionic
villus sampling (CVS) – the removal
(under continuous ultrasound guidance) of a
small amount
of placental tissue, either transabdominally or transvaginally, to test for chromosomal problems
or genetic disorders. |
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Genetic
Counseling – An approximately one-hour
appointment with a genetic counselor or geneticist
to discuss
prenatal diagnostic choices and individual risks
of genetic problems. |
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First-trimester
combined screening – involves
a fetal ultrasound combined with a blood test
to indicate
if your
pregnancy is at a higher chance for Down syndrome,
Trisomy 13, or Trisomy
18. |
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Second-trimester
serum screening [COMING SOON] – a blood
test which measures four fetal chemical markers
and screens for Down syndrome, Trisomy 18, and
open neural tube defects. |
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Sequential
screening [COMING SOON] – similar to
integrated screening, except that interim
results are
available after the first trimester ultrasound and blood test. If there is a very low risk
of Down syndrome, a second trimester blood
test may not be necessary. |
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Integrated
screening [COMING SOON] – involves an
ultrasound and a blood test in the first trimester,
followed
by a blood test in the second trimester, to
assess your risk for Down syndrome, Trisomy
18, and open neural tube defects. |
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