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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

The maximum days the report can be obtained for the Chromosomal Microarray (CMA-HD) Test is typically within 14-21 days after the sample is received in the laboratory.

What are the prerequisites for the test Chromosomal Microarray (CMA-HD) Test

  • Written consent is required from the patient or legal guardian.
  • Physician order for the test.
  • Specimen collection kit provided by the testing laboratory.
  • Specimen sample (blood or tissue) collected by a healthcare provider.
  • Proper labeling of the specimen with patient information.

What are the measure values for the test Chromosomal Microarray (CMA-HD) Test

  • Measure 1: Copy Number Variations (CNVs) - This measure detects gains or losses of genetic material in the form of duplications or deletions in chromosomes.
  • Measure 2: Loss of Heterozygosity (LOH) - This measure identifies regions of chromosomes where there is loss of one allele due to chromosomal rearrangements.
  • Measure 3: Uniparental Disomy (UPD) - This measure detects regions of chromosomes where both copies are inherited from the same parent instead of one from each parent.
  • Measure 4: Mosaicism - This measure identifies genetic abnormalities that are present in only a subset of cells in an individual.

What does this test Chromosomal Microarray (CMA-HD) Test identify?

Chromosomal Microarray (CMA-HD) Test Identification

The Chromosomal Microarray (CMA-HD) Test is a genetic test that identifies various genetic abnormalities at a high resolution. This test specifically looks for copy number variations (CNVs) in the DNA, which are changes in the number of copies of a particular gene or region of DNA. CNVs can include deletions, duplications, and other rearrangements of genetic material.

Some of the conditions that the CMA-HD Test can identify include:

  • Genetic syndromes
  • Developmental delays
  • Autism spectrum disorders
  • Intellectual disabilities
  • Birth defects

The test can also help in diagnosing conditions such as Down syndrome, DiGeorge syndrome, Prader-Willi syndrome, and Angelman syndrome, among others. Overall, the CMA-HD Test is a powerful tool for identifying genetic abnormalities that may be contributing to a patient's symptoms or condition.

Why is this test Chromosomal Microarray (CMA-HD) Test taken?

The Chromosomal Microarray (CMA-HD) Test is taken to detect any genetic abnormalities or chromosomal imbalances in an individual. This test is especially helpful in diagnosing genetic disorders, developmental delays, intellectual disabilities, and birth defects. By analyzing the entire genome at a high resolution, the CMA-HD test can identify even small genetic changes that may be missed by other tests.

Popular FAQs on Test

A Chromosomal Microarray (CMA-HD) Test is a genetic test that looks for extra or missing pieces of chromosomes that may be too small to be seen under a microscope.
A CMA-HD Test is done to diagnose genetic conditions, developmental delays, intellectual disabilities, and birth defects. It can also be used to determine the cause of pregnancy loss or infertility.
A CMA-HD Test is performed using a blood sample or tissue sample. The sample is sent to a laboratory where the DNA is analyzed for chromosomal abnormalities.
Coverage for a CMA-HD Test may vary depending on the insurance provider and the reason for the test. It is recommended to check with your insurance company prior to having the test done.
The risks of a CMA-HD Test are minimal and include the possibility of discomfort during sample collection and the rare chance of infection or bleeding at the site of collection.

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