Max Lab > Lab Test in Noida > Lab Test in P 1 > Non Invasive Prenatal Aneuploidies Screening (NIPT) Test
₹ 15000
10% OFF for Senior Citizens | USE CODE SS10 *
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Non Invasive Prenatal Aneuploidies Screening (NIPT) Test |
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Blood |
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Sample by Monday 10 PM Report by 5 Days |
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₹ 15000 |
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Description
The Non-invasive Prenatal Testing (NIPT) is a prenatal screening test in P 1, Noida used to detect potential chromosomal abnormalities and other fetal health concerns. It provides expectant parents with early insights into their baby's genetic health. NIPT is a blood test in P 1, Noida recommended for all pregnant women, but especially those in certain categories with a higher risk of chromosomal abnormalities.
The NIPT Test is a sensitive screening test in P 1, Noida that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
NIPT lab test in P 1, Noidas can also detect abnormalities in sex chromosomes and other genetic conditions. While it's a valuable tool, it's important to remember:
NIPT is a screening test in P 1, Noida: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in P 1, Noidaing may be needed.
NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.
NIPT blood test in P 1, Noida reports can help in determining the sex of the fetus. Moreover, a non-invasive prenatal paternity test can be performed as early as the 7th week of pregnancy to determine the paternity of the fetus.
Unlike other invasive test in P 1, Noidas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in P 1, Noida poses no risk to the fetus.
Chromosomal abnormalities can happen during fetal development or egg/sperm formation due to errors in cell division (meiosis or mitosis). While maternal age is a risk factor, these abnormalities can occur in pregnancies regardless of age or health history.
NIPT test can scan several key abnormalities and help doctors and parents-to-be to prepare for and manage pregnancy more effectively.
While there are no outward signs that indicate chromosomal disorders, pregnancies that are at a higher risk conditions include,
Description
The Non-invasive Prenatal Testing (NIPT) is a prenatal screening test in P 1, Noida used to detect potential chromosomal abnormalities and other fetal health concerns. It provides expectant parents with early insights into their baby's genetic health. NIPT is a blood test in P 1, Noida recommended for all pregnant women, but especially those in certain categories with a higher risk of chromosomal abnormalities.
The NIPT Test is a sensitive screening test in P 1, Noida that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
NIPT lab test in P 1, Noidas can also detect abnormalities in sex chromosomes and other genetic conditions. While it's a valuable tool, it's important to remember:
NIPT is a screening test in P 1, Noida: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in P 1, Noidaing may be needed.
NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.
NIPT blood test in P 1, Noida reports can help in determining the sex of the fetus. Moreover, a non-invasive prenatal paternity test can be performed as early as the 7th week of pregnancy to determine the paternity of the fetus.
Unlike other invasive test in P 1, Noidas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in P 1, Noida poses no risk to the fetus.
Chromosomal abnormalities can happen during fetal development or egg/sperm formation due to errors in cell division (meiosis or mitosis). While maternal age is a risk factor, these abnormalities can occur in pregnancies regardless of age or health history.
NIPT test can scan several key abnormalities and help doctors and parents-to-be to prepare for and manage pregnancy more effectively.
While there are no outward signs that indicate chromosomal disorders, pregnancies that are at a higher risk conditions include,
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