
Get the Non-invasive Prenatal Screening with Cell-free DNA
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Comprehensive Prenatal Screening Program Physician Referral Form 1901 Outlet Center Dr. Suite 120 Oxnard CA 93036Tel: 805.604.9500 Fax: 805.604.9559 www.PalmsImaging.comPATIENT INFORMATION Name (Last/First/MI)://Phone
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01
Step 1: Before starting the non-invasive prenatal screening, gather all the necessary information and documents such as medical history, previous test results, and any specific instructions provided by your healthcare provider.
02
Step 2: Schedule an appointment with a qualified healthcare professional who specializes in prenatal screening.
03
Step 3: During the appointment, the healthcare professional will explain the procedure and obtain your consent for the screening.
04
Step 4: The healthcare professional will draw a small amount of blood from your arm.
05
Step 5: The blood sample will be sent to a laboratory for analysis.
06
Step 6: The laboratory will perform genetic testing on the blood sample to identify any abnormalities or genetic conditions in the fetus.
07
Step 7: Once the results are available, the healthcare professional will discuss the findings with you and explain any further steps or recommendations.
08
Step 8: Follow any additional instructions or recommendations given by your healthcare provider to ensure the well-being of both you and your baby.
Who needs non-invasive prenatal screening with?
01
Non-invasive prenatal screening is recommended for pregnant women who may have a higher risk of having a baby with chromosomal disorders or genetic conditions, such as advanced maternal age (35 years or older), previous pregnancy with chromosomal abnormality, family history of genetic conditions, or abnormal ultrasound findings.
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What is non-invasive prenatal screening with?
Non-invasive prenatal screening is a method used to analyze the DNA of a pregnant woman's blood to assess the risk of certain chromosomal conditions in the fetus.
Who is required to file non-invasive prenatal screening with?
Non-invasive prenatal screening may be recommended for pregnant women who are at increased risk for chromosomal abnormalities or genetic disorders in the fetus.
How to fill out non-invasive prenatal screening with?
Non-invasive prenatal screening is typically done by collecting a blood sample from the pregnant woman and sending it to a laboratory for analysis.
What is the purpose of non-invasive prenatal screening with?
The purpose of non-invasive prenatal screening is to provide information to the pregnant woman and her healthcare provider about the risk of chromosomal abnormalities in the fetus.
What information must be reported on non-invasive prenatal screening with?
Non-invasive prenatal screening reports typically include the risk assessment for conditions such as Down syndrome, trisomy 18, and trisomy 13.
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