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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

The maximum days the report can be obtained for the test Karyotyping + QF-PCR (Basic) + CMA (750K) Package is 21 days.

What are the prerequisites for the test Karyotyping + QF-PCR (Basic) + CMA (750K) Package

  • Karyotyping:
    • No specific prerequisites
  • QF-PCR (Basic):
    • No fasting required
    • Inform the healthcare provider about any medications being taken
  • CMA (750K):
    • No specific prerequisites
    • Inform the healthcare provider about any medications being taken

What are the measure values for the test Karyotyping + QF-PCR (Basic) + CMA (750K) Package

  • Karyotyping: Yes
  • QF-PCR (Basic): Yes
  • CMA (750K): Yes

What does this test Karyotyping + QF-PCR (Basic) + CMA (750K) Package identify?

  • Karyotyping: This test is used to identify any abnormalities in the structure or number of chromosomes in a person's cells. It can detect conditions such as Down syndrome, Turner syndrome, and Klinefelter syndrome.
  • QF-PCR (Basic): This test is a rapid and accurate method for detecting common chromosomal abnormalities, such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome).
  • CMA (750K): This test, also known as Chromosomal Microarray Analysis, is a high-resolution genetic test that can detect microdeletions and microduplications in the genome. It can identify genetic disorders that may not be detected by traditional karyotyping or QF-PCR.

Why is this test Karyotyping + QF-PCR (Basic) + CMA (750K) Package taken?

This test package is taken to provide a comprehensive analysis of an individual's genetic makeup. Karyotyping is used to examine the structure and number of chromosomes, which can help identify chromosomal abnormalities such as Down syndrome or Turner syndrome. QF-PCR is a rapid test that can detect common chromosomal disorders such as trisomy 21, 18, and 13. CMA (750K) is a high-resolution test that can detect smaller chromosomal abnormalities, including microdeletions and duplications.

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