Veritas NIPT Basic – Non-Invasive Prenatal Test for Early Genetic Screening

AED1,050.00

Veritas NIPT Basic is a non-invasive prenatal test (NIPT) that screens for common chromosomal abnormalities, including trisomy 21 (Down syndrome), trisomy 18, and trisomy 13, using a simple maternal blood sample. It offers high accuracy, early detection from the 10th week of pregnancy, and a low false-positive rate, reducing the need for invasive procedures. The test is safe for both mother and baby, providing fast and reliable results to support informed pregnancy decisions.

Sample Type : Maternal blood
Methodology : NGS
TAT : 10 Days

Description

Veritas NIPT Basic: Comprehensive Non-Invasive Prenatal Testing for Early Genetic Insights

The Veritas NIPT Basic is a cutting-edge non-invasive prenatal test (NIPT) designed to provide expectant parents with critical insights into their baby’s genetic health. Using advanced Next-Generation Sequencing (NGS) technology, this test analyzes fetal DNA from a simple maternal blood sample to screen for common chromosomal abnormalities, including trisomies such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). With a turnaround time of just 10 days, the Veritas NIPT Basic offers a safe, accurate, and timely solution for early genetic screening during pregnancy.

### Why You Need This Test
The Veritas NIPT Basic is essential for expectant parents seeking peace of mind and proactive management of their pregnancy. This test is particularly important for identifying chromosomal abnormalities that could impact the baby’s development. Early detection allows parents and healthcare providers to make informed decisions about prenatal care, delivery planning, and potential interventions. Unlike invasive procedures like amniocentesis, the Veritas NIPT Basic is completely non-invasive, posing no risk to the mother or baby.

This test is especially recommended for women who are at higher risk of chromosomal abnormalities due to factors such as advanced maternal age (35 years or older), a history of chromosomal conditions in the family, or abnormal findings in routine ultrasounds or blood tests. By choosing the Veritas NIPT Basic, you can take control of your pregnancy journey with confidence and clarity.

Veritas NIPT Basic### Symptoms That Indicate This Test
While the Veritas NIPT Basic is not symptom-driven, it is highly recommended in the following scenarios:
– Advanced maternal age (35 years or older).
– A family history of genetic or chromosomal conditions.
– Abnormal results from first-trimester screening tests or ultrasounds.
– Previous pregnancies affected by chromosomal abnormalities.
– Parental concerns about genetic health and early detection.

### Natural Production
During pregnancy, small fragments of fetal DNA, known as cell-free DNA (cfDNA), circulate in the mother’s bloodstream. This cfDNA is naturally released from the placenta and provides valuable genetic information about the developing baby. The Veritas NIPT Basic analyzes this cfDNA to detect chromosomal abnormalities with high accuracy. Factors such as maternal age, weight, and gestational age can influence the levels of cfDNA, which is why this test is most effective after 10 weeks of pregnancy.

### What Happens If Untreated
Ignoring potential chromosomal abnormalities can lead to significant challenges for both the baby and the parents. Conditions like Down syndrome, Edwards syndrome, and Patau syndrome can affect the baby’s physical and intellectual development, requiring specialized medical care and long-term support. Early detection through the Veritas NIPT Basic allows parents to prepare emotionally, medically, and financially for any potential outcomes. It also enables healthcare providers to optimize prenatal care and delivery planning, ensuring the best possible outcomes for both mother and baby.

### How to Prepare for the Test
The Veritas NIPT Basic requires no special preparation. You do not need to fast or make any dietary changes before the test. However, it is important to inform your healthcare provider about any medications or supplements you are taking, as well as any relevant medical history. The test is typically performed after 10 weeks of pregnancy to ensure accurate results.

### Test Overview
Sample Type: Maternal blood.
Methodology: Next-Generation Sequencing (NGS).
Turnaround Time (TAT): 10 days.

The Veritas NIPT Basic is a molecular diagnostic test that uses state-of-the-art NGS technology to analyze fetal DNA with exceptional precision. The test is performed on a small blood sample drawn from the mother, making it a safe and convenient option for prenatal screening. Results are typically available within 10 days, providing timely insights to support informed decision-making.

Take control of your pregnancy journey with the Veritas NIPT Basic. This non-invasive prenatal test offers unparalleled accuracy and peace of mind, empowering you to make informed decisions about your baby’s health. Don’t wait—book your lab test today and gain valuable insights into your baby’s genetic health. The Veritas NIPT Basic is your trusted solution for early genetic screening.

Category: Molecular Diagnostics

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