QF PCR Panel 131821XY Test
Cost: AED 1200.0
Test Components: Sterile container, Sterile Normal Saline Container, EDTA Vacutainer
Sample Condition: Amniotic fluid, Chorionic villi, Cord Blood
Report Delivery: 1-2 days
Method: Sanger Sequencing
Test Type: Genetics
Doctor: Gynecologist
Test Department: DNA Labs UAE
Pre Test Information
The QF PCR Panel 131821XY Test can be done with a doctor’s prescription. However, the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details
The QF PCR Panel 131821XY Test is a diagnostic test used to detect certain genetic abnormalities. It is specifically designed to identify numerical abnormalities in chromosomes 13, 18, and 21, as well as abnormalities in the sex chromosomes (XY).
Chromosomal abnormalities in these regions can lead to various genetic disorders, such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
The QF PCR Panel is commonly used in prenatal testing to screen for these conditions in fetuses. The test works by analyzing the DNA present in a sample, typically obtained through amniocentesis or chorionic villus sampling.
The DNA is amplified using a technique called quantitative fluorescent polymerase chain reaction (QF PCR), which allows for the detection of specific chromosomal abnormalities.
The results of the QF PCR Panel can provide valuable information to healthcare providers and parents, allowing for appropriate counseling and management of pregnancies affected by genetic abnormalities.
Test Name | QF PCR Panel 131821XY Test |
---|---|
Components | Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer |
Price | 1200.0 AED |
Sample Condition | Amniotic fluid\/ Chorionic villi\/ Cord Blood |
Report Delivery | 1-2 days |
Method | Sanger Sequencing |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | QF PCR Panel 13,18,21,XY] can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
The QF PCR Panel [13,18,21,XY] is a diagnostic test used to detect certain genetic abnormalities. It is specifically designed to identify numerical abnormalities in chromosomes 13, 18, and 21, as well as abnormalities in the sex chromosomes (XY). Chromosomal abnormalities in these regions can lead to various genetic disorders, such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). The QF PCR Panel is commonly used in prenatal testing to screen for these conditions in fetuses. The test works by analyzing the DNA present in a sample, typically obtained through amniocentesis or chorionic villus sampling. The DNA is amplified using a technique called quantitative fluorescent polymerase chain reaction (QF PCR), which allows for the detection of specific chromosomal abnormalities. The results of the QF PCR Panel can provide valuable information to healthcare providers and parents, allowing for appropriate counseling and management of pregnancies affected by genetic abnormalities. |