Get the free Prenatal Genetic Screen - Southeast Womens Center OBGYN

Prenatal Genetic Screen Southeast Women's Center Name Patient # Date 1. Will you be 35 years or older when the baby is due? Yes No 2. Have you, the babies father, or anyone in either of your families

How to fill out prenatal genetic screen

How to fill out prenatal genetic screen:

1. Start by scheduling an appointment with your healthcare provider who specializes in prenatal care. They will guide you through the process and provide all necessary instructions.
2. Obtain any necessary paperwork or forms from your healthcare provider. These forms will typically require your personal information, medical history, and family history.
3. Review the forms carefully and fill them out accurately. Provide any necessary details about previous pregnancies, medical conditions, or genetic disorders that may run in your family.
4. Determine the type of prenatal genetic screening you wish to undergo. There are various options available, such as noninvasive prenatal screening (NIPS), carrier testing, or diagnostic testing. Discuss these options with your healthcare provider to determine which is most suitable for your situation.
5. If you opt for noninvasive prenatal screening (NIPS), a simple blood test is typically performed. This test analyzes the fetal DNA in your blood to identify the risk of certain chromosomal abnormalities, such as Down syndrome, Edwards syndrome, or Patau syndrome.
6. If you choose carrier testing, your healthcare provider will take a blood sample or perform a cheek swab to analyze your DNA for specific genetic disorders that you or your partner may be carriers of. This type of screening helps determine the likelihood of passing on genetic conditions to your baby.
7. In the case of diagnostic testing, such as amniocentesis or chorionic villus sampling (CVS), your healthcare provider will discuss the procedure, potential risks, and benefits with you before proceeding. These tests involve sampling fetal tissue or amniotic fluid to diagnose genetic abnormalities with a high level of certainty.

Who needs prenatal genetic screen:

1. Pregnant women who have a family history of genetic disorders or birth defects may benefit from prenatal genetic screening. This allows them to assess the risk of passing on these conditions to their unborn child.
2. Women who are over the age of 35 are generally recommended to undergo prenatal genetic screening. Advanced maternal age is associated with an increased risk of chromosomal abnormalities like Down syndrome.
3. Couples who have previously had a child with a genetic disorder may also choose to undergo prenatal genetic screening to assess the risk for future pregnancies.
4. Prenatal genetic screening is also recommended for individuals who belong to certain ethnic or racial groups that are at higher risk for specific genetic conditions. For example, individuals of Ashkenazi Jewish descent may opt for carrier testing to identify the risk of conditions like Tay-Sachs disease.

It is important to consult with your healthcare provider to determine if prenatal genetic screening is appropriate for you and to ensure that you have a clear understanding of the process and its potential outcomes.

For pdfFiller’s FAQs

What is prenatal genetic screen?

Prenatal genetic screening is a test done during pregnancy to assess a baby's risk of having certain genetic disorders.

Who is required to file prenatal genetic screen?

Pregnant women are typically required to undergo prenatal genetic screening.

How to fill out prenatal genetic screen?

Prenatal genetic screening is usually performed by a healthcare provider through a blood test or ultrasound.

What is the purpose of prenatal genetic screen?

The purpose of prenatal genetic screening is to identify any potential genetic disorders or abnormalities in the fetus.

What information must be reported on prenatal genetic screen?

Prenatal genetic screening reports typically include information about the mother's health, family history, and any test results.

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