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Reports Within

Parameters

Reports Within:

Parameter Include:

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

Maximum Days for Report:

  • NIPT- All Chromosomes + Microdeletions Test
  • Maximum days to obtain report: 7-10 business days

What are the prerequisites for the test NIPT- All Chromosomes + Microdeletions Test

  • Confirmation of singleton pregnancy
  • Gestational age of at least 10 weeks
  • Maternal age of 18 years or older
  • Availability of fetal fraction for testing
  • Maternal weight of at least 100 lbs
  • No history of organ transplantation
  • No history of bone marrow transplantation

What are the measure values for the test NIPT- All Chromosomes + Microdeletions Test

  • Chromosome 1: Normal
  • Chromosome 2: Normal
  • Chromosome 3: Normal
  • Chromosome 4: Normal
  • Chromosome 5: Normal
  • Chromosome 6: Normal
  • Chromosome 7: Normal
  • Chromosome 8: Normal
  • Chromosome 9: Normal
  • Chromosome 10: Normal
  • Chromosome 11: Normal
  • Chromosome 12: Normal
  • Chromosome 13: Normal
  • Chromosome 14: Normal
  • Chromosome 15: Normal
  • Chromosome 16: Normal
  • Chromosome 17: Normal
  • Chromosome 18: Normal
  • Chromosome 19: Normal
  • Chromosome 20: Normal
  • Chromosome 21: Normal
  • Chromosome 22: Normal
  • Chromosome X: Normal
  • Chromosome Y: Normal
  • Microdeletion 1: Not Detected
  • Microdeletion 2: Not Detected
  • Microdeletion 3: Not Detected

What does this test NIPT- All Chromosomes + Microdeletions Test identify?

NIPT- All Chromosomes + Microdeletions Test

The NIPT- All Chromosomes + Microdeletions Test is a non-invasive prenatal screening test that identifies chromosomal abnormalities and microdeletions in the fetus. This test analyzes the fetal DNA circulating in the mother's bloodstream to detect any abnormalities.

The test specifically looks for abnormalities in all 23 pairs of chromosomes, including sex chromosomes X and Y. It also identifies microdeletions, which are small missing pieces of genetic material that can cause developmental issues in the fetus.

Overall, the NIPT- All Chromosomes + Microdeletions Test provides comprehensive information about the genetic health of the fetus, helping to assess the risk of genetic disorders such as Down syndrome, Edwards syndrome, and Patau syndrome, as well as microdeletion syndromes like DiGeorge syndrome and Prader-Willi syndrome.

Why is this test NIPT- All Chromosomes + Microdeletions Test taken?

NIPT- All Chromosomes + Microdeletions Test is taken to screen for chromosomal abnormalities and microdeletions in the fetus during pregnancy. This test is typically recommended for women who are at increased risk of having a baby with genetic disorders, such as advanced maternal age or a history of chromosomal abnormalities in previous pregnancies. By analyzing the fetal DNA in the mother's blood, this test can provide information about the baby's risk of conditions such as Down syndrome, trisomy 18, trisomy 13, and certain microdeletion syndromes.

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