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Beta Thalassemia-HBB Full Gene Analysis Single Test Cost

Original price was: 2,000 د.إ.Current price is: 1,500 د.إ.

-25%

Beta Thalassemia-HBB Full Gene Analysis Single Test at DNA Labs UAE is a comprehensive genetic screening designed to identify mutations in the HBB gene, which is responsible for beta-thalassemia, a blood disorder that reduces the production of hemoglobin. Hemoglobin is the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. Mutations in the HBB gene can lead to various forms of beta-thalassemia, ranging from mild to severe, affecting an individual’s quality of life and requiring different management strategies.

This test is particularly valuable for individuals with a family history of beta-thalassemia or those belonging to ethnic groups with a high prevalence of the disease. It’s also crucial for couples considering starting a family, as it can help assess the risk of passing the condition to their offspring.

Performed at the state-of-the-art DNA Labs UAE, the test involves a simple blood draw. The laboratory utilizes advanced genetic sequencing techniques to thoroughly analyze the HBB gene for any mutations that could lead to beta-thalassemia. The cost of the test is set at 1500 AED, making it an accessible option for those seeking comprehensive insights into their genetic health regarding beta-thalassemia.

Results from this test can provide crucial information for diagnosis, informing treatment plans, and making informed decisions about family planning. It is a valuable tool in the proactive management of beta-thalassemia, offering individuals and families peace of mind and the opportunity to plan for the future with greater certainty.

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Beta Thalassemia-HBB Full Gene Analysis Single Test

Test Name: Beta Thalassemia-HBB Full Gene Analysis Single Test

Components: EDTA Vacutainer (2ml)

Price: 1500.0 AED

Sample Condition: Peripheral blood

Report Delivery: 8-10 days

Method: Sanger Sequencing

Test Type: Genetics

Doctor: Gynecologist

Test Department:

Pre Test Information: Beta Thalassemia-HBB Full Gene Analysis (Single) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details:

Beta thalassemia is a genetic disorder characterized by reduced production of hemoglobin, the protein in red blood cells that carries oxygen. It is caused by mutations in the HBB gene, which provides instructions for making the beta-globin protein, a component of hemoglobin.

A beta thalassemia-HBB full gene analysis is a genetic test that examines the entire HBB gene to identify any mutations or variations that may be causing the disorder. This analysis involves sequencing the gene’s DNA to identify specific changes in the nucleotide sequence that may disrupt the normal function of the gene.

The results of this analysis can provide valuable information about the specific mutations present in an individual’s HBB gene and help determine the severity of the beta thalassemia condition. This information can be used for genetic counseling, family planning, and to guide treatment decisions.

Test Name Beta Thalassemia-HBB Full Gene Analysis Single Test
Components EDTA Vacutainer (2ml)
Price 1500.0 AED
Sample Condition Peripheral blood
Report Delivery 8-10 days
Method Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Beta Thalassemia-HBB Full Gene Analysis (Single) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Beta thalassemia is a genetic disorder characterized by reduced production of hemoglobin, the protein in red blood cells that carries oxygen. It is caused by mutations in the HBB gene, which provides instructions for making the beta-globin protein, a component of hemoglobin.

A beta thalassemia-HBB full gene analysis is a genetic test that examines the entire HBB gene to identify any mutations or variations that may be causing the disorder. This analysis involves sequencing the gene’s DNA to identify specific changes in the nucleotide sequence that may disrupt the normal function of the gene.

The results of this analysis can provide valuable information about the specific mutations present in an individual’s HBB gene and help determine the severity of the beta thalassemia condition. This information can be used for genetic counseling, family planning, and to guide treatment decisions.