Name: Non Invasive Prenatal Aneuploidies Screening (NIPT) Test Price in Panchkula
Brand: Max Lab
SKU: 68189
Price: 15000 INR
Availability: InStock
Rating: 4.8 (6988 reviews)

Home > Lab Tests in Panchkula > Non Invasive Prenatal Aneuploidies Screening (NIPT) Test

Description
- The Non-invasive Prenatal Testing (NIPT) is a prenatal screening test in 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 Panchkula recommended for all pregnant women, but especially those in certain categories with a higher risk of chromosomal abnormalities.

The Non-invasive Prenatal Testing (NIPT) is a prenatal screening test in 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 Panchkula recommended for all pregnant women, but especially those in certain categories with a higher risk of chromosomal abnormalities.

Overview of the NIPT

The NIPT Test is a sensitive screening test in Panchkula that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).

NIPT lab test in 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 Panchkula: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in Panchkulaing may be needed.

NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.

NIPT blood test in 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 Panchkulas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in 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,

The mother is 35 years or older at the time of gestation.
Ultrasound reveals potential abnormalities.
Serum screen test in Panchkulas are positive.
Past pregnancies with aneuploidy disorder.
A family history of genetic disorders.
Biological parents are blood relatives.
History of infertility or recurrent miscarriages.

Overview of the NIPT

The NIPT Test is a sensitive screening test in Panchkula that primarily assesses the condition of Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).

NIPT lab test in 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 Panchkula: It indicates an increased risk of an abnormality, but it's not diagnostic. Further test in Panchkulaing may be needed.

NIPT doesn't detect all abnormalities: It focuses on specific chromosomal conditions.

Unlike other invasive test in Panchkulas like Chorionic villus sampling (CVS), amniocentesis, and percutaneous umbilical blood sampling, a basic NIPT test in Panchkula poses no risk to the fetus.

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,

The mother is 35 years or older at the time of gestation.
Ultrasound reveals potential abnormalities.
Serum screen test in Panchkulas are positive.
Past pregnancies with aneuploidy disorder.
A family history of genetic disorders.
Biological parents are blood relatives.
History of infertility or recurrent miscarriages.

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Test Name :	Non Invasive Prenatal Aneuploidies Screening (NIPT) Test
Sample Type :	Blood
Gender :	Female
Age group :	All Age Groups
Pre-test Instruction :	Doctor Prescription is must
This Test Includes :	Non Invasive Prenatal Aneuploidies Screening (NIPT) 1 Tests

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Non Invasive Prenatal Aneuploidies Screening (NIPT) Test Includes:
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