Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test
At DNA Labs UAE, we offer the Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test for genetic analysis. This test is used to detect chromosomal abnormalities in a fetus or an individual.
Test Details
The Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test involves analyzing the DNA of a sample obtained from various sources such as amniotic fluid, chorionic villus sampling, cord blood, products of conception, or peripheral blood. The technology used is Microarray Affymetrix and Cell Culture.
Test Components
- Sterile Container/ Sterile Normal Saline Container/EDTA & Heparinised vacutainer (3 ml each)
Test Price
The cost of the Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test is 5400.0 AED.
Sample Condition
The test can be performed on samples of amniotic fluid, chorionic villi, products of conception, cord blood, or peripheral blood.
Report Delivery
The report for the test will be delivered within 7-9 days.
Method
The Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test utilizes a DNA chip or microarray to detect variations in the number of copies of DNA segments across the genome. It can detect changes in the number of copies of genes or entire chromosomes, such as deletions, duplications, or rearrangements.
Test Type
The Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test falls under the category of genetics.
Doctor
This test is typically ordered by a gynecologist.
Test Department
This test is conducted in the genetics department.
Pre Test Information
Microarray 750K and Single Karyotyping (AF/CVS/CB/POC/PB) can be done with a doctor’s prescription. However, a prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Symptoms and Diagnosis
The Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test is used to diagnose genetic disorders such as Down syndrome, Turner syndrome, or DiGeorge syndrome. It can also identify genetic predispositions to certain conditions, such as cancer or cardiovascular disease.
Conclusion
The Microarray 750K and Single Karyotyping AFCVSCBPOCPB Test offered by DNA Labs UAE is a powerful tool for prenatal and postnatal diagnosis of genetic disorders. It provides a comprehensive evaluation of the genetic status of the sample and can help guide clinical management and treatment decisions.
Test Name | Microarray 750Kand Single Karyotyping AFCVSCBPOCPB Test |
---|---|
Components | Sterile Container/ Sterile Normal Saline Container/EDTA & Heparinised vacutainer (3 ml each) |
Price | 5400.0 AED |
Sample Condition | Amniotic fluid\/ Chorionic villi\/Products of Conception\/Cord blood\/Peripheral blood |
Report Delivery | 7-9 days |
Method | Microarray Affymetrix]+ Cell Culture |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | Microarray 750K+ Single Karyotyping (AF/CVS/CB/POC/PB) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details | Microarray 750K+ Single Karyotyping is a genetic testing technique that is used to detect chromosomal abnormalities in a fetus or an individual. It involves analyzing the DNA of a sample obtained from various sources such as amniotic fluid (AF), chorionic villus sampling (CVS), cord blood (CB), products of conception (POC), or peripheral blood (PB). The microarray 750K+ technology utilizes a DNA chip or microarray to detect variations in the number of copies of DNA segments across the genome. It can detect changes in the number of copies of genes or entire chromosomes, such as deletions, duplications, or rearrangements. Single karyotyping is a complementary test that can confirm the results of microarray analysis. It involves analyzing the chromosomes of the sample under a microscope to detect any structural abnormalities. This combined testing approach provides a comprehensive evaluation of the genetic status of the sample and can help diagnose genetic disorders such as Down syndrome, Turner syndrome, or DiGeorge syndrome. It can also identify genetic predispositions to certain conditions, such as cancer or cardiovascular disease. Overall, microarray 750K+ Single Karyotyping is a powerful tool for prenatal and postnatal diagnosis of genetic disorders and can help guide clinical management and treatment decisions. |