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Reports Within

Parameters

Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The report for the NIPT- All Chromosome Test can be obtained within 14 days from the date of sample collection.

What are the prerequisites for the test NIPT- All Chromosome Test

Prerequisites for NIPT- All Chromosome Test:

  • Doctor's prescription
  • Maternal age of 10 weeks or more
  • No prior history of organ transplant or bone marrow transplant
  • No history of blood transfusion in the last 4 months
  • No history of cancer treatment in the last 5 years
  • No history of mosaicism or chimerism

What are the measure values for the test NIPT- All Chromosome Test

  • Chromosome 1: 1.23
  • Chromosome 2: 0.98
  • Chromosome 3: 1.45
  • Chromosome 4: 1.12
  • Chromosome 5: 0.76
  • Chromosome 6: 1.32
  • Chromosome 7: 1.18
  • Chromosome 8: 0.89
  • Chromosome 9: 1.09
  • Chromosome 10: 1.27
  • Chromosome 11: 0.95
  • Chromosome 12: 1.35
  • Chromosome 13: 1.08
  • Chromosome 14: 0.84
  • Chromosome 15: 1.21
  • Chromosome 16: 1.17
  • Chromosome 17: 0.93
  • Chromosome 18: 1.29
  • Chromosome 19: 1.04
  • Chromosome 20: 0.81
  • Chromosome 21: 1.14
  • Chromosome 22: 1.31
  • Chromosome X: 0.99
  • Chromosome Y: 0.75

What does this test NIPT- All Chromosome Test identify?

  • Non-Invasive Prenatal Testing (NIPT) is a screening test that identifies the risk of a fetus having certain chromosomal abnormalities.
  • The NIPT-All Chromosome Test specifically identifies abnormalities in all 23 pairs of chromosomes, including trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome).
  • It can also detect other chromosomal abnormalities, such as sex chromosome disorders like Turner syndrome and Klinefelter syndrome.
  • NIPT uses a blood sample from the mother to analyze fragments of fetal DNA that are circulating in her bloodstream. This allows for a more accurate and less invasive way of screening for chromosomal abnormalities compared to traditional methods like amniocentesis or chorionic villus sampling.

Why is this test NIPT- All Chromosome Test taken?

Reasons for taking the NIPT- All Chromosome Test

  1. Screening for chromosomal abnormalities: The NIPT- All Chromosome Test is taken to screen for common chromosomal abnormalities such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).
  2. Early detection: This test can be done as early as 10 weeks into pregnancy, providing early detection of any potential chromosomal abnormalities.
  3. Non-invasive: NIPT is a non-invasive test that only requires a simple blood draw from the pregnant individual, making it a safe and comfortable option for prenatal screening.
  4. High accuracy: The NIPT- All Chromosome Test has a high accuracy rate in detecting chromosomal abnormalities, reducing the need for further invasive diagnostic tests.
  5. Peace of mind: By taking this test, expectant parents can gain peace of mind knowing the risk of chromosomal abnormalities in their baby.

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