NIPT NonInvasive Pregnancy Genetic DNA Test
د.إ 2,000.00 د.إ 1,500.00 Book Now
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NIPT NonInvasive Pregnancy Genetic DNA Test

د.إ 2,000.00 د.إ 1,500.00

-25%

The Non – Invasive Prenatal Test (NIPT) is a DNA test on maternal blood to safely and reliably screen pregnancies for the most common fetal aneuploidies Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome) and Trisomy 13 (Patau syndrome).

Samples : At least 10 ml blood in a specific blood tube (STRECK) is required from the mother. The maternal blood can be taken from week 10 of the pregnancy.

(50 customer reviews)

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Description

Did you know that fragments of your baby’s DNA circulate in baby’s mother bloodstream during pregnancy?

NIPT Test is a safe, accurate and affordable Non-Invasive Prenatal Test (NIPT) that screens for the three most common chromosomal abnormalities:

  1. Down syndrome (trisomy 21)
  2. Edwards syndrome (trisomy 18)
  3. Patau syndrome (trisomy 13)

NIPT Test gives you and your doctor important information in the earliest stage of pregnancy and is more accurate than conventional screening methods. NIPT Test helps you to avoid unnecessary, risky invasive procedures such as amniocentesis and chorionic villus sampling.

Down syndrome 

The most common, well-known genetic abnormality is Down syndrome, caused by the presence of a third copy of chromosome 21. Approximately 22 in 10,000 babies are born with Down syndrome. It is associated with delayed physical development, typical facial features and mild to moderate intellectual disability.

Edwards syndrome

Edwards syndrome, also known as trisomy 18, is caused by an additional copy of chromosome 18. Edwards syndrome occurs in around one in every 6,000 pregnancies. Babies with this syndrome rarely survive due to abnormalities of the heart, kidneys and other internal organs.

Patau syndrome

Patau syndrome, also known as trisomy 13, is caused by an additional copy of chromosome 13. Like babies with trisomy 18, babies with trisomy 13 also have multiple birth defects and often dont survive the first few months.

  • Simple: Blood sample from the mother
  • Reliable: Screens for Down, Edwards and Patau syndrome
  • Safe: Risk-free for the pregnancy

NIPT Test can be performed as early as 8 weeks gestation. It poses no risk to you or to your baby. NIPT Test requires a standard blood sample drawn from the mother’s arm. The sample is sent to a local lab where an expert analyzes the DNA of the fetus for signs of trisomy of chromosomes 21, 18 and 13.

STEP 1: The doctor draws a blood sample from the mother’s arm. The blood sample contains cell-free DNA from the mother and the fetus.

STEP 2: The blood sample is sent to the local laboratory and analyzed for:

  1. Down syndrome (trisomy 21)
  2. Edwards syndrome (trisomy 18)
  3. Patau syndrome (trisomy 13)

STEP 3: The laboratory sends the test results to your doctor.

STEP 4: Your doctor explains the results and provides counselling about further prenatal care.

Prenatal screening can reassure you about the development of your baby. If the NIPT Test detects Down, Edwards or Patau syndrome, your doctor may recommend an additional diagnostic test to confirm the result.

50 reviews for NIPT NonInvasive Pregnancy Genetic DNA Test

  1. shaikh sana

    excellent service

  2. sunny

    happy with their results and sample collection service

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