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Get the Cell free fetal DNA blood test for Down Syndrome

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NIP REQUEST Foretell free fetal DNA blood test for Down Syndrome MEMBER OF THE LED NETWORK Dr. Stephen Sennett MBBS FRANZCRDiploma Fetal Medicine(London) Provider No. 221533EKDr. Bridget Sutton MBBS
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Collect blood sample from pregnant woman
02
Separate the cell-free fetal DNA from the maternal blood
03
Perform DNA extraction and analysis to detect and analyze the fetal DNA

Who needs cell fetal dna blood?

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Cell-free fetal DNA blood testing is typically recommended for pregnant women who are at higher risk for genetic abnormalities in the fetus, such as women over the age of 35 or those with a family history of genetic disorders.
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Cell-free fetal DNA blood testing is a noninvasive prenatal testing method that analyzes fetal DNA in the mother's blood to screen for certain chromosomal abnormalities.
Pregnant women who are looking to screen for chromosomal abnormalities in their unborn child are typically required to undergo cell-free fetal DNA blood testing.
Cell-free fetal DNA blood testing involves having a blood sample drawn from the pregnant woman, which is then sent to a laboratory for analysis. The results are typically provided to the healthcare provider who can discuss them with the expectant mother.
The purpose of cell-free fetal DNA blood testing is to screen for chromosomal abnormalities, such as Down syndrome, in the unborn child without the need for invasive procedures like amniocentesis or chorionic villus sampling.
Cell-free fetal DNA blood testing reports typically include the risk assessment for specific chromosomal abnormalities, such as trisomy 21, trisomy 18, and trisomy 13.
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