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Chromosomal Microarray CMA 750K High Resolution Test

5,150 د.إ

-10%

The Chromosomal Microarray (CMA) 750K High Resolution Test is a cutting-edge genetic test offered by DNA Labs UAE, designed to detect chromosomal abnormalities with unparalleled precision. This test examines the entire genome at a high resolution of 750,000 markers, allowing for the identification of microdeletions and duplications that traditional karyotyping methods might miss. These anomalies can be linked to a wide range of genetic disorders and developmental delays, making this test a valuable tool for early diagnosis and intervention.

With a cost of 5150 AED, the CMA 750K High Resolution Test is an investment in obtaining a comprehensive genetic overview, which can be particularly beneficial for individuals with unexplained developmental issues, autism, intellectual disabilities, or congenital anomalies. Conducted at the state-of-the-art facilities of DNA Labs UAE, this test requires a simple blood sample from which DNA is extracted and analyzed. The results provide detailed insights into one’s chromosomal health, offering a roadmap for personalized medical management and informed family planning decisions.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test

Test Name: CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test

Components: Blood

Price: 5150.0 AED

Report Delivery: 2 weeks

Method: Affymetrix CytoScan? 750K Microarray

Test Type: Genetic Disorders

Doctor: Pediatrician, Physician, Gynecologist

Test Department: CYTOGENETICS

Pre Test Information: Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.

Test Details

The Chromosomal Microarray (CMA) 750K High Resolution Test is a genetic test that uses advanced technology to detect and analyze small genetic changes in an individual’s DNA. The test is designed to identify copy number variations (CNVs), which are changes in the number of copies of a particular DNA segment.

The CMA 750K test uses a high-density microarray platform to analyze over 750,000 genetic markers across the entire genome. This high level of resolution allows for the detection of very small CNVs, as well as the identification of CNVs in regions of the genome that were previously difficult to analyze.

The CMA 750K test is typically used in clinical settings to diagnose genetic disorders, such as developmental delays, intellectual disability, autism spectrum disorders, and congenital anomalies. It can also be used to identify genetic factors that may increase an individual’s risk for certain diseases or conditions.

Overall, the CMA 750K test provides a powerful tool for understanding the genetic basis of disease and can help inform treatment decisions and genetic counseling.

Test Name CHROMOSOMAL MICROARRAY CMA 750K HIGH RESOLUTION Test
Components
Price 5150.0 AED
Sample Condition Blood
Report Delivery 2 weeks
Method Affymetrix CytoScan? 750K Microarray
Test type Genetic Disorders
Doctor Pediatrician, Physician, Gynecologist
Test Department: CYTOGENETICS
Pre Test Information Duly filled Genomic Microarray Requisition Form (Form 19) is mandatory.
Test Details

The Chromosomal Microarray (CMA) 750K High Resolution Test is a genetic test that uses advanced technology to detect and analyze small genetic changes in an individual’s DNA. The test is designed to identify copy number variations (CNVs), which are changes in the number of copies of a particular DNA segment.

The CMA 750K test uses a high-density microarray platform to analyze over 750,000 genetic markers across the entire genome. This high level of resolution allows for the detection of very small CNVs, as well as the identification of CNVs in regions of the genome that were previously difficult to analyze.

The CMA 750K test is typically used in clinical settings to diagnose genetic disorders, such as developmental delays, intellectual disability, autism spectrum disorders, and congenital anomalies. It can also be used to identify genetic factors that may increase an individual’s risk for certain diseases or conditions.

Overall, the CMA 750K test provides a powerful tool for understanding the genetic basis of disease and can help inform treatment decisions and genetic counseling.