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. |