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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

The maximum days the report can be obtained for the test Karyotyping + QF-PCR (Basic) + CMA (315K) Test is 21 days.

What are the prerequisites for the test Karyotyping + QF-PCR (Basic) + CMA (315K) Test

  • Patient must have a referral from a healthcare provider
  • Must have signed consent form for testing
  • Must have completed pre-test counseling

What are the measure values for the test Karyotyping + QF-PCR (Basic) + CMA (315K) Test

  • Karyotyping: Yes
  • QF-PCR (Basic): Yes
  • CMA (315K): Yes

What does this test Karyotyping + QF-PCR (Basic) + CMA (315K) Test identify?

  • Karyotyping: This test examines the chromosomes in a sample of cells to identify any abnormalities in the number or structure of chromosomes. It can detect conditions such as Down syndrome, Turner syndrome, and Klinefelter syndrome.
  • QF-PCR (Basic): Quantitative Fluorescent Polymerase Chain Reaction (QF-PCR) is a rapid method used to detect common chromosomal abnormalities, such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome).
  • CMA (315K): Chromosomal Microarray Analysis (CMA) is a high-resolution genetic test that can detect small deletions or duplications in the genome. The 315K refers to the number of markers used in the analysis, which allows for a more detailed assessment of genetic abnormalities.

Why is this test Karyotyping + QF-PCR (Basic) + CMA (315K) Test taken?

Reasons for taking the Karyotyping + QF-PCR (Basic) + CMA (315K) Test

1. Karyotyping: This test is used to examine the chromosomes in a sample of cells to determine if there are any abnormalities or genetic disorders present. It can help diagnose conditions such as Down syndrome, Turner syndrome, and Klinefelter syndrome.

2. QF-PCR (Quantitative Fluorescent Polymerase Chain Reaction): This test is often performed in conjunction with karyotyping to provide more detailed information about specific chromosomal abnormalities. It can help confirm the presence of certain genetic conditions and provide additional insights into the genetic makeup of an individual.

3. CMA (Comparative Genomic Hybridization Microarray): This test is a high-resolution genetic analysis that can detect smaller genetic abnormalities that may not be visible with traditional karyotyping. It can identify deletions, duplications, and other structural changes in the DNA that may be associated with developmental delays, intellectual disabilities, or other genetic conditions.

By combining these three tests, healthcare providers can obtain a comprehensive evaluation of an individual's genetic profile and identify any potential chromosomal abnormalities or genetic disorders that may be present.

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