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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

Maximum Report Turnaround Time for Test FISH (5 Probe) + CMA (315K) + MCC Package

The maximum days to obtain the report for the test FISH (5 Probe) + CMA (315K) + MCC Package is 14 days.

What are the prerequisites for the test FISH (5 Probe) + CMA (315K) + MCC Package

  • FISH (5 Probe) test
  • CMA (315K) test
  • MCC Package

What are the measure values for the test FISH (5 Probe) + CMA (315K) + MCC Package

Test Measure Values
FISH (5 Probe) Positive
CMA (315K) Normal
MCC Package Positive

What does this test FISH (5 Probe) + CMA (315K) + MCC Package identify?

This test includes Fluorescence In Situ Hybridization (FISH) with 5 probes, Chromosomal Microarray Analysis (CMA) with a resolution of 315K, and Multiplex Ligation-dependent Probe Amplification (MLPA) for identifying chromosomal abnormalities at a molecular level.

FISH is a cytogenetic technique used to detect and localize the presence or absence of specific DNA sequences on chromosomes. In this test, 5 probes are used to target specific regions of interest on the chromosomes, helping to identify genetic abnormalities such as deletions, duplications, or translocations.

CMA is a high-resolution genomic technique that allows for the detection of submicroscopic chromosomal imbalances. With a resolution of 315K, CMA can identify small deletions or duplications in the genome that may be missed by conventional karyotyping. This test is particularly useful for diagnosing genetic disorders and syndromes.

The MCC (Molecular Cytogenetics Consortium) Package combines FISH, CMA, and MLPA to provide a comprehensive analysis of chromosomal abnormalities at both the cytogenetic and molecular levels. This integrated approach allows for a more accurate and detailed assessment of genetic variations, helping to guide clinical decision-making and personalized treatment strategies.

Why is this test FISH (5 Probe) + CMA (315K) + MCC Package taken?

Reasons for taking the FISH (5 Probe) + CMA (315K) + MCC Package test:

1. Comprehensive genetic testing: The FISH (5 Probe) test is used to detect specific genetic abnormalities in a sample. The CMA (315K) test, on the other hand, is a more comprehensive test that looks for a wider range of genetic abnormalities. By combining these tests, a more thorough analysis of the genetic material can be conducted.

2. Increased accuracy: By using multiple testing methods, the likelihood of detecting genetic abnormalities is increased. This can provide a more accurate diagnosis and treatment plan for the individual undergoing testing.

3. Medical condition evaluation: The MCC Package includes additional tests and consultations that can help in the evaluation of a medical condition. This comprehensive approach can provide a more holistic view of the individual's health status.

4. Personalized treatment plan: The results of these tests can help in developing a personalized treatment plan for the individual based on their genetic profile. This can lead to more effective and targeted treatment options.

Popular FAQs on Test

The FISH (5 Probe) + CMA (315K) + MCC Package test is a comprehensive genetic testing package that combines Fluorescence In Situ Hybridization (FISH) with Chromosomal Microarray Analysis (CMA) and Multiplex Ligation-dependent Probe Amplification (MLPA) to provide a detailed analysis of genetic abnormalities.
The purpose of this test is to identify genetic abnormalities, such as chromosomal deletions, duplications, and rearrangements, that may be associated with various genetic disorders and syndromes.
The FISH (5 Probe) test involves using fluorescently labeled DNA probes to detect specific chromosomal abnormalities, while the CMA (315K) test analyzes the entire genome for copy number variations. The MCC Package test combines these two techniques for a more comprehensive analysis.
This test can detect a wide range of genetic abnormalities, including microdeletions, microduplications, unbalanced translocations, and other chromosomal rearrangements that are associated with genetic disorders such as Down syndrome, DiGeorge syndrome, and Prader-Willi syndrome.
This test is typically recommended for individuals who have a family history of genetic disorders, recurrent pregnancy losses, developmental delays, or congenital abnormalities. It may also be recommended for couples undergoing fertility treatments or prenatal screening.

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