Max Lab > Lab Test in Panchkula > Lab Test in Sector2 > 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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₹ 15000 |
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Description
The Non-invasive Prenatal Testing (NIPT) is a prenatal screening test in Sector2, Panchkula 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 Sector2, Panchkula 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 Sector2, Panchkula that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
NIPT lab test in Sector2, Panchkulas 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 Sector2, Panchkula: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in Sector2, Panchkulaing may be needed.
NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.
NIPT blood test in Sector2, Panchkula 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 Sector2, Panchkulas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in Sector2, Panchkula 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 Sector2, Panchkula 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 Sector2, Panchkula 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 Sector2, Panchkula that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
NIPT lab test in Sector2, Panchkulas 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 Sector2, Panchkula: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in Sector2, Panchkulaing may be needed.
NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.
NIPT blood test in Sector2, Panchkula 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 Sector2, Panchkulas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in Sector2, Panchkula 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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