Alpha Thalassemia HBA1-HBA2 Deletion-Duplication Analysis Test
Test Name: Alpha thalassemia HBA1 – HBA2 deletion-duplication analysis test
Components: Blood EDTA Tube
Price: 2600.0 AED
Report Delivery: 2 to 3 Weeks
Method: Hematology
Doctor: Hematologist
Test Department: Genetics
Pre Test Information: Requires HBA1-HBA2 gene to be detected for further analysis
Test Details
The Alpha thalassemia HBA1 – HBA2 deletion-duplication analysis test is a genetic test that is used to detect deletions or duplications in the HBA1 and HBA2 genes. These genes are responsible for producing alpha-globin chains, which are essential components of hemoglobin.
Alpha thalassemia is a genetic disorder characterized by a reduced production of alpha-globin chains, leading to an imbalance in the production of hemoglobin. This imbalance can result in a range of symptoms, including anemia and other complications.
The deletion-duplication analysis test involves analyzing the DNA of an individual to determine if there are any deletions or duplications in the HBA1 and HBA2 genes. This is typically done using a technique called polymerase chain reaction (PCR), which amplifies specific regions of the DNA for analysis.
By detecting deletions or duplications in the HBA1 and HBA2 genes, the test can help diagnose alpha thalassemia and determine the specific type and severity of the condition. This information is important for guiding treatment decisions and providing genetic counseling to affected individuals and their families.
It is important to note that the Alpha thalassemia HBA1 – HBA2 deletion-duplication analysis test specifically looks for deletions or duplications in the HBA1 and HBA2 genes and is not a comprehensive test for all types of alpha thalassemia. Other genetic tests may be necessary to fully evaluate an individual for alpha thalassemia.
| Test Name | Alpha thalassemia HBA1 – HBA2 deletion-duplication analysis Test |
|---|---|
| Components | |
| Price | 2600.0 AED |
| Sample Condition | Blood EDTA Tube |
| Report Delivery | 2 to 3 Weeks |
| Method | |
| Test type | Hematology |
| Doctor | Hematologist |
| Test Department: | Genetics |
| Pre Test Information | Requires HBA1-HBA2 gene to be detected for further analysis |
| Test Details |
The Alpha thalassemia HBA1 HBA2 deletion-duplication analysis test is a genetic test that is used to detect deletions or duplications in the HBA1 and HBA2 genes. These genes are responsible for producing alpha-globin chains, which are essential components of hemoglobin. Alpha thalassemia is a genetic disorder characterized by a reduced production of alpha-globin chains, leading to an imbalance in the production of hemoglobin. This imbalance can result in a range of symptoms, including anemia and other complications. The deletion-duplication analysis test involves analyzing the DNA of an individual to determine if there are any deletions or duplications in the HBA1 and HBA2 genes. This is typically done using a technique called polymerase chain reaction (PCR), which amplifies specific regions of the DNA for analysis. By detecting deletions or duplications in the HBA1 and HBA2 genes, the test can help diagnose alpha thalassemia and determine the specific type and severity of the condition. This information is important for guiding treatment decisions and providing genetic counseling to affected individuals and their families. It is important to note that the Alpha thalassemia HBA1 HBA2 deletion-duplication analysis test specifically looks for deletions or duplications in the HBA1 and HBA2 genes and is not a comprehensive test for all types of alpha thalassemia. Other genetic tests may be necessary to fully evaluate an individual for alpha thalassemia. |
