Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test
At DNA Labs UAE, we offer the Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test for genetic analysis. This test is designed to identify any chromosomal abnormalities in fetal cells obtained from amniocentesis or chorionic villus sampling (CVS).
Test Components
- Sterile Container/ Sterile Normal Saline Container
Price
5200.0 AED
Sample Condition
Amniotic fluid/ Chorionic villi
Report Delivery
7-9 days
Method
Microarray Agilent + Cell Culture + FISH
Test Type
Genetics
Doctor
Gynecologist
Test Department
Pre Test Information
Microarray 60K (AF/CVS) + Karyotyping + FISH chromosome 21 can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details
Microarray 60K (AF/CVS) is a genetic test that analyzes a small sample of fetal cells obtained from either amniocentesis or chorionic villus sampling (CVS) to identify any chromosomal abnormalities. This test can detect a wide range of chromosomal disorders, including Down syndrome, Turner syndrome, and Edwards syndrome.
Karyotyping is another genetic test that examines the chromosomes in a sample of fetal cells to detect any abnormalities. This test involves growing the cells in a laboratory and staining them to visualize the chromosomes under a microscope. Karyotyping can detect larger chromosomal abnormalities, such as deletions, duplications, and translocations.
FISH (fluorescence in situ hybridization) chromosome 21 is a specific type of genetic test that uses fluorescent probes to identify any abnormalities on chromosome 21. This test is often used in conjunction with other genetic tests, such as microarray and karyotyping, to confirm a diagnosis of Down syndrome.
Together, these three tests provide a comprehensive evaluation of the fetal chromosomes and can help identify any genetic abnormalities that may affect the health of the developing fetus.
Test Name | Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test |
---|---|
Components | Sterile Container/ Sterile Normal Saline Container |
Price | 5200.0 AED |
Sample Condition | Amniotic fluid\/ Chorionic villi |
Report Delivery | 7-9 days |
Method | Microarray Agilent]+ Cell Culture+ FISH |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | Microarray 60K (AF/CVS) + Karyotyping + FISH chromosome 21 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 60K (AF/CVS) is a genetic test that analyzes a small sample of fetal cells obtained from either amniocentesis or chorionic villus sampling (CVS) to identify any chromosomal abnormalities. This test can detect a wide range of chromosomal disorders, including Down syndrome, Turner syndrome, and Edwards syndrome. Karyotyping is another genetic test that examines the chromosomes in a sample of fetal cells to detect any abnormalities. This test involves growing the cells in a laboratory and staining them to visualize the chromosomes under a microscope. Karyotyping can detect larger chromosomal abnormalities, such as deletions, duplications, and translocations. FISH (fluorescence in situ hybridization) chromosome 21 is a specific type of genetic test that uses fluorescent probes to identify any abnormalities on chromosome 21. This test is often used in conjunction with other genetic tests, such as microarray and karyotyping, to confirm a diagnosis of Down syndrome. Together, these three tests provide a comprehensive evaluation of the fetal chromosomes and can help identify any genetic abnormalities that may affect the health of the developing fetus. |