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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

Maximum Days to Obtain Report for CMA 315K + FISH (3 Probes- 21, X & Y)

Maximum Days to Obtain Report for Test CMA 315K + FISH (3 Probes- 21, X & Y)

The maximum days to obtain the report for the test CMA 315K + FISH (3 Probes- 21, X & Y) is typically 10-14 working days.

What are the prerequisites for the test CMA 315K + FISH (3 Probes- 21, X & Y)

  • CMA 315K test
  • FISH test with 3 probes - 21, X, and Y

What are the measure values for the test CMA 315K + FISH (3 Probes- 21, X & Y)

  • CMA 315K + FISH (3 Probes- 21, X & Y) Test Measures:
  • - Probe 21: Value
  • - Probe X: Value
  • - Probe Y: Value

What does this test CMA 315K + FISH (3 Probes- 21, X & Y) identify?

Test: CMA 315K + FISH (3 Probes - 21, X & Y)

The CMA 315K test, combined with FISH analysis using three probes targeting chromosomes 21, X, and Y, is utilized to identify chromosomal abnormalities and genetic disorders in individuals. This test is particularly useful in detecting conditions such as Down syndrome (Trisomy 21), Turner syndrome (Monosomy X), Klinefelter syndrome (XXY), and other chromosomal disorders.

The CMA 315K test involves chromosomal microarray analysis, which allows for the detection of submicroscopic chromosomal imbalances that may not be visible under a microscope. This analysis provides detailed information about the structure and number of chromosomes in an individual's genome, helping to identify genetic abnormalities that may be associated with developmental delays, intellectual disabilities, birth defects, and other medical conditions.

By combining the CMA 315K test with FISH analysis using probes specific to chromosomes 21, X, and Y, healthcare providers can obtain a comprehensive assessment of an individual's chromosomal profile and identify any abnormalities that may be present. This information is crucial for accurate diagnosis, prognosis, and treatment planning for patients with suspected genetic disorders.

Why is this test CMA 315K + FISH (3 Probes- 21, X & Y) taken?

Test: CMA 315K + FISH (3 Probes- 21, X & Y)

This test is taken to diagnose genetic abnormalities or chromosomal disorders in individuals. The test combines Chromosomal Microarray Analysis (CMA) with Fluorescence In Situ Hybridization (FISH) using three specific probes for chromosomes 21, X, and Y.

CMA is a high-resolution genetic test that can detect small deletions or duplications in the genome, which are often missed by other tests. It is particularly useful in identifying genetic causes for developmental delays, intellectual disabilities, autism spectrum disorders, and other genetic conditions.

FISH is a technique that uses fluorescently labeled DNA probes to visualize specific regions of chromosomes. By using probes for chromosomes 21, X, and Y, this test can identify abnormalities in these chromosomes, such as trisomies, monosomies, deletions, or translocations.

By combining CMA with FISH using these specific probes, healthcare providers can accurately diagnose chromosomal disorders and provide appropriate treatment and genetic counseling to individuals and their families.

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