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Get the free Non Invasive Prenatal Test (NIPT) Pathology Request

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Place ULTRA barcode replace LATER collection kit barcode Harmon Invasive Prenatal Test (NIP) Pathology Request 12PATIENT INFORMATIONPatient Name (Last, First): DOB (DD/Month/YYY): Address: ORDERING
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How to fill out non invasive prenatal test

01
To fill out a non-invasive prenatal test, follow these steps:
02
Consult with your healthcare provider: Schedule an appointment with your doctor or genetic counselor to discuss the need for a non-invasive prenatal test.
03
Provide your medical history: During the appointment, provide detailed information about your medical history, previous pregnancies, and any genetic conditions that may be present in your family.
04
Blood sample collection: The non-invasive prenatal test requires a blood sample from the pregnant woman. A healthcare professional will take a small sample of your blood using a needle.
05
Laboratory testing: The collected blood sample will be sent to a specialized laboratory where it will be tested for genetic abnormalities in the fetus.
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Wait for the results: It usually takes a few weeks for the laboratory to analyze the sample and generate the test results.
07
Interpretation of results: Once the results are available, your healthcare provider will explain the findings, including any potential risks or abnormalities detected.
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Follow-up consultations: Based on the results, your healthcare provider will guide you on the appropriate next steps and provide necessary support or further testing if required.

Who needs non invasive prenatal test?

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The non-invasive prenatal test is recommended for the following individuals:
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- Pregnant women who are considered at higher risk for certain genetic disorders or chromosomal abnormalities.
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- Individuals with a family history of genetic conditions or chromosomal abnormalities.
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- Women who have had previous pregnancies with genetic disorders or birth defects.
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- Pregnant women over the age of 35, as advanced maternal age increases the risk of certain genetic conditions.
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- Couples who have undergone fertility treatments or assisted reproductive technologies.
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- Individuals who want to gather more information about the genetic health of their unborn child for personal reasons.
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Non-invasive prenatal testing (NIPT) is a screening test that examines the DNA of a baby in the mother's blood to assess the risk of certain genetic conditions.
Pregnant women who want to assess the risk of genetic conditions in their baby may choose to undergo NIPT.
NIPT involves a simple blood draw from the mother, which is then sent to a laboratory for analysis.
The purpose of NIPT is to provide information about the risk of genetic conditions in the baby, allowing parents to make informed decisions about further testing or pregnancy management.
The NIPT report usually includes information about the risk of certain genetic conditions such as Down syndrome, trisomy 18, and trisomy 13.
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