NIPT- All Chromosome Test in Bangalore

NIPT- All Chromosome Test in Bangalore

NIPT, or Non-Invasive Prenatal Test, analyzes the odds of chromosomal abnormalities in a developing fetus's DNA. The DNA detects genetic conditions, such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). This helps your healthcare provider know the risk of genetic conditions. The test can be done in the first 10 weeks of pregnancy. 

Prescribed and performed specifically during pregnancy, the NIPT Test analyzes cell-free DNA in the mother's blood. Doctors may often suggest this NIPT Test when there is a high risk of chromosomal abnormalities. The NIPT test is called cell-free DNA (cfDNA) screening or noninvasive prenatal test(NIPT). The test is important to identify the risk of having genetic disorders in the fetus. The test has options and does not diagnose particular conditions. Getting tested in time may help you identify the risk and take preventive measures to save you from potential complications. So, if your doctor has suggested the NIPT - All Chromosome Testing, contact Redcliffe Labs. You can book the NIPT Test in Bangalore online in just 1 minute and get your reports within a stipulated time frame.

Test Details:

NIPT- All Chromosome Test Cost in Different Cities - Redcliffe Labs

Note: We also offer NIPT- All Chromosome Test PAN India. Please call the number 8988988787 to check the availability of our services in your area.

Reasons When Do Doctors Suggest A NIPT Blood Test:

• Doctors might recommend a NIPT Blood Test when:
• Women have an advanced maternal age (35 or over)
• Has had a history of pregnancy with a chromosomal abnormality
• Have abnormal ultrasound findings
• Those who have positive First Trimester screening
• Have had a family history of chromosomal abnormalities

It is about the safety of you and your baby, do not delay and book a NIPT Blood Test in Bangalore with Healthy India Ki Trusted Lab, Redcliffe Labs today.

Purpose Of NIPT Test:

• It helps identify chromosomal abnormalities in the fetus
• Provide information about the baby's health at an earlier stage
• Pose a minimal risk to both the mother and the fetus
• Demonstrate high sensitivity and specificity
• Help healthcare providers make informed decisions

Doctors will suggest NIPT Testing based on individual circumstances, and additional testing may be needed depending on the test results. Following the instructions and getting tested in time is essential to take control of one's health in time. If the test is suggested, and you are looking for an NIPT test near me, book an NIPT Blood Test near me with us now.

Who should get genetic testing?

The prenatal test is not mandatory. Your doctor may recommend the NIPT test if they are unsure about the condition. The test results provide important information about the health status of the fetus. Doctors recommend that all pregnant women take genetic screening as part of their pregnancy care. Here are some people who should take this NIPT Test during pregnancy- 

• Irregular result of a genetic screening test
• Family or personal history of genetic conditions.
• Pregnancy over age 35.
• History of miscarriage or stillbirth.

How is the NIPT test done?

Your healthcare provider collects your blood sample during the NIPT test. A small amount of the fetus's DNA circulates in your blood during pregnancy. The NIPT test detects fragments of fetal DNA in the blood, known as cell-free DNA (cfDNA). 

The healthcare provider collects the blood sample from the vein in your arm and sends it to the lab to analyze the specific conditions. 

What is the NIPT Test Screen for?

The NIPT test does not detect any chromosomal disorders; the test detects the risk of- 

• Trisomy 13
• Down syndrome (trisomy 21)
• Disorders affecting sex chromosomes (X and Y)
• Trisomy 18

An extra chromosome may cause various genetic disorders, including syndrome, trisomy 18, and trisomy 13. The test screens the sex chromosomes and looks for differences in the number of sex chromosomes. The most common sex chromosome disorders are Klinefelter syndrome, Turner syndrome, Triple X syndrome, and XYY syndrome. 

What do the results of the NIPT test mean?

The test does not provide a yes or no answer regarding whether the fetus has a condition. The noninvasive prenatal screening test indicates the risk of fetal chromosomal abnormalities. Consult your doctor to interpret your test results.

If the test indicates positive results, it means that the fetus has a higher risk of developing a genetic disorder.

However, a negative result means the fetus is at a low risk of developing a genetic disorder.

Your healthcare provider may suggest other tests, including Amniocentesis and chorionic villus sampling (CVS), to understand your condition and determine the next steps. They may also refer you to a genetic counselor to understand your risk of pregnancies and genetic conditions.

Is it mandatory to get genetic testing during pregnancy?

No, the NIPT test is not mandatory. However, it is your choice, and your doctor may recommend it based on your medical history. Parents and their doctors are free to choose whether to undergo prenatal screening or diagnostic testing. 

When should the NIPT test be done in pregnancy?

NIPT testing can be done during the early weeks of pregnancy. It is recommended from 10 weeks through delivery.