Genetic counseling at MedStar Health helps identify the risk of having a baby with birth defects, mental retardation, or an inherited disease. Genetic counseling may occur either before or during a pregnancy. The process begins with a genetic counselor reviewing the parents' family, medical and obstetric histories. From this information, the counselor can determine and explain the possible genetic risks a couple may face in their pregnancy.
Not every couple needs genetic counseling, but those with certain risk factors may find genetic counseling and testing helpful. Risk factors include:
Pregnancy at the age of 35 or older
A history of multiple miscarriages
A family history of a genetic disease
A family history of mental retardation or birth defects
Exposure to certain medications or drugs during pregnancy
An ethnic or racial background in which a certain genetic disorder is more common (i.e. - sickle cell disease for African-Americans)
Once risks have been identified, a genetic counselor will discuss tests that are available to you and your baby. Certain blood tests may be offered to determine if parents are carriers for hereditary disorders. Other tests may be offered during the pregnancy to assess the baby for specific problems. These fetal diagnostic procedures may include:
Amniocentesis: the sampling of amniotic fluid using a hollow needle inserted into the uterus, to screen for developmental abnormalities in a fetus
Biophysical profiles: a prenatal test used to check on a baby's well-being using fetal heart rate monitoring (non-stress test) and fetal ultrasound
Chorionic villus sampling: a prenatal test that involves taking a sample of some of the placental tissue to test for chromosomal abnormalities and some other genetic problems
Detailed fetal ultrasound: an imaging technique that uses high-frequency sound waves to produce images of a baby in the uterus which can be used to evaluate possible problems or confirm a diagnosis
Maternal serum screening (MSS): a blood test available to pregnant women to help determine the risk of Down syndrome, Edward syndrome or neural tube defects
Ultrasound for Nuchal translucency: and ultrasound used to measure a collection of fluid under the skin at the back of your baby's neck to determine whether or not a baby is likely to have Down's syndrome
Your counselor will discuss the benefits and risks of these procedures, and how to proceed.
Make an Appointment
For more information or to schedule an appointment with a women's health specialist, call our scheduling line or use the online request form below:
At MedStar Georgetown, our women's health specialists coordinate care with your primary care physician to make sure you receive the best care over the long term. Learn more.