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Alpha Thalassemia Gene Analysis HBA1 – HBA2 Test Cost

Original price was: 6,000 د.إ.Current price is: 4,800 د.إ.

-20%

Alpha Thalassemia Gene Analysis HBA1 – HBA2 Test is a specialized diagnostic procedure aimed at detecting mutations in the HBA1 and HBA2 genes, which are crucial for the production of the alpha globin component of hemoglobin. Hemoglobin is a protein in red blood cells responsible for transporting oxygen throughout the body. Mutations in these genes can lead to alpha thalassemia, a blood disorder that reduces the production of normal hemoglobin, leading to anemia and other related health issues.

The test is performed by collecting a blood sample from the patient, which is then analyzed using advanced genetic testing techniques to identify any abnormalities or mutations in the HBA1 and HBA2 genes. This test is particularly important for individuals with a family history of thalassemia or those belonging to ethnic groups with a higher prevalence of the disease, as it can help in early diagnosis and management of the condition.

Offered by DNA Labs UAE, the Alpha Thalassemia Gene Analysis HBA1 – HBA2 Test is priced at 4800 AED. DNA Labs UAE is known for its state-of-the-art facilities and expert team of geneticists and medical professionals who ensure accurate and reliable test results. The test is an essential tool in the management and treatment planning of alpha thalassemia, providing vital information for affected individuals and their families.

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Alpha Thalassemia Gene Analysis HBA1 – HBA2 Test

Test Name: Alpha Thalassemia Gene Analysis HBA1 – HBA2 Test

Components: Hematology

Price: 4800.0 AED

Sample Condition: Blood EDTA Tube

Report Delivery: 2 to 3 Weeks

Method: Test Type

Doctor: Hematologist

Test Department: Genetics

Pre Test Information: Requires HBA1-HBA2 gene to be detected for further analysis

Test Details

The alpha thalassemia gene analysis HBA1-HBA2 test is a genetic test that looks for changes or mutations in the HBA1 and HBA2 genes that are responsible for producing alpha globin chains in hemoglobin. Alpha thalassemia is a genetic disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. The severity of the disorder depends on the number of gene mutations present.

The HBA1-HBA2 test is used to diagnose alpha thalassemia and to determine the number of gene mutations present. The test is performed using a blood sample and analyzes the DNA of the HBA1 and HBA2 genes to look for changes or mutations. There are four types of alpha thalassemia, each with different levels of severity. The HBA1-HBA2 test can determine if an individual has one or more gene mutations and can help predict the severity of the disorder.

If an individual has one gene mutation, they may have mild or no symptoms. If they have two gene mutations, they may have moderate to severe symptoms, including anemia, fatigue, and jaundice. If they have three or four gene mutations, the disorder can be life-threatening and require regular blood transfusions.

The HBA1-HBA2 test is typically ordered by a healthcare provider if an individual has symptoms of alpha thalassemia or has a family history of the disorder. The results of the test can help guide treatment and management of the disorder.

Test Name Alpha thalassemia gene analysis HBA1 – HBA2 Test
Components
Price 4800.0 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 gene analysis HBA1-HBA2 test is a genetic test that looks for changes or mutations in the HBA1 and HBA2 genes that are responsible for producing alpha globin chains in hemoglobin. Alpha thalassemia is a genetic disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. The severity of the disorder depends on the number of gene mutations present.

The HBA1-HBA2 test is used to diagnose alpha thalassemia and to determine the number of gene mutations present. The test is performed using a blood sample and analyzes the DNA of the HBA1 and HBA2 genes to look for changes or mutations.

There are four types of alpha thalassemia, each with different levels of severity. The HBA1-HBA2 test can determine if an individual has one or more gene mutations and can help predict the severity of the disorder.

If an individual has one gene mutation, they may have mild or no symptoms. If they have two gene mutations, they may have moderate to severe symptoms, including anemia, fatigue, and jaundice. If they have three or four gene mutations, the disorder can be life-threatening and require regular blood transfusions.

The HBA1-HBA2 test is typically ordered by a healthcare provider if an individual has symptoms of alpha thalassemia or has a family history of the disorder. The results of the test can help guide treatment and management of the disorder.

SKU: TEST-892 Category:

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