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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 test Karyotyping + QF-PCR (Basic) + CMA (315K) + MCC Package can be obtained within 15-20 business days from the date of sample collection.

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

  • Karyotyping: None required
  • QF-PCR (Basic): None required
  • CMA (315K): None required
  • MCC Package: None required

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

  • Karyotyping: Included
  • QF-PCR (Basic): Included
  • CMA (315K): Included
  • MCC Package: Included

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

  • Karyotyping: This test is used to analyze the number, size, and shape of chromosomes in a sample of cells. It can identify chromosomal abnormalities such as aneuploidy (extra or missing chromosomes) or structural rearrangements.
  • QF-PCR (Quantitative Fluorescent Polymerase Chain Reaction): This test specifically looks for common aneuploidies such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome) by measuring the amount of specific DNA sequences present in the sample.
  • CMA (Comparative Genomic Hybridization Microarray): This test analyzes the entire genome for submicroscopic chromosomal imbalances, including deletions, duplications, and other structural changes that may not be detected by traditional karyotyping.
  • MCC (Microarray Chromosome Copy Number Analysis): This package combines the QF-PCR and CMA tests to provide a comprehensive analysis of chromosomal abnormalities, including common aneuploidies and submicroscopic imbalances.

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

Reason for taking the test package: Karyotyping + QF-PCR (Basic) + CMA (315K) + MCC Package

This test package is recommended for individuals who may have a higher risk of genetic disorders or chromosomal abnormalities. Here is a breakdown of each component of the test and why it is included:

  • Karyotyping: This test examines the number and structure of chromosomes in a sample of cells. It can help identify chromosomal abnormalities such as Down syndrome, Turner syndrome, and Klinefelter syndrome.
  • QF-PCR (Basic): Quantitative Fluorescent Polymerase Chain Reaction (QF-PCR) is a rapid and accurate method for detecting common chromosomal aneuploidies, such as trisomy 21 (Down syndrome), trisomy 18, and trisomy 13.
  • CMA (315K): Chromosomal Microarray Analysis (CMA) is a high-resolution genetic test that can detect small deletions or duplications in the genome. It is particularly useful for identifying genetic syndromes and developmental delays.
  • MCC Package: This component likely includes additional counseling and consultation services to help individuals understand their test results and make informed decisions about their healthcare options.

By combining these tests, healthcare providers can obtain a comprehensive evaluation of an individual's genetic makeup and identify any potential risks or abnormalities. This information can be crucial for guiding medical management and providing personalized care.

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