HBB Gene Sickle Cell Anemia Genetic Test
At DNA Labs UAE, we offer the HBB Gene Sickle Cell Anemia Genetic Test at a cost of AED 4400.0. This test is essential for individuals who suspect they may have sickle cell anemia or have a family history of the condition.
Test Components
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Hematology
- Doctor: Hematologist
- Test Department: Genetics
Pre Test Information
Before undergoing the HBB Gene Sickle Cell Anemia Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by the HBB Gene Sickle Cell Anemia NGS Genetic DNA Test gene HBB.
Test Details
The HBB gene is responsible for encoding the beta-globin protein, a component of hemoglobin. Sickle cell anemia is a genetic disorder caused by a mutation in the HBB gene. This mutation leads to the production of abnormal hemoglobin molecules, which can cause red blood cells to become misshapen and prone to clumping. This can result in various symptoms such as chronic anemia, pain crises, and organ damage.
NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of sickle cell anemia, an NGS genetic test can be used to identify mutations in the HBB gene that are associated with the disorder. This test can provide information about the specific genetic variant causing sickle cell anemia in an individual, allowing for accurate diagnosis and genetic counseling.
NGS genetic testing for sickle cell anemia can be particularly useful in carrier screening, prenatal testing, and pre-implantation genetic diagnosis. It can help identify individuals who carry a single copy of the mutated HBB gene and are at risk of passing the disorder to their children. Additionally, NGS testing can be used to identify the presence of the HBB gene mutation in embryos created through in vitro fertilization, allowing for the selection of embryos without the mutation for implantation.
Overall, NGS genetic testing for the HBB gene in sickle cell anemia can provide valuable information for diagnosis, family planning, and reproductive decision-making.
| Test Name | HBB Gene Sickle cell anemia Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Hematology |
| Doctor | Hematologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for HBB Gene Sickle cell anemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBB Gene Sickle cell anemia NGS Genetic DNA Test gene HBB |
| Test Details |
The HBB gene is responsible for encoding the beta-globin protein, a component of hemoglobin. Sickle cell anemia is a genetic disorder caused by a mutation in the HBB gene. This mutation leads to the production of abnormal hemoglobin molecules, which can cause red blood cells to become misshapen and prone to clumping. This can result in various symptoms such as chronic anemia, pain crises, and organ damage. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of sickle cell anemia, an NGS genetic test can be used to identify mutations in the HBB gene that are associated with the disorder. This test can provide information about the specific genetic variant causing sickle cell anemia in an individual, allowing for accurate diagnosis and genetic counseling. NGS genetic testing for sickle cell anemia can be particularly useful in carrier screening, prenatal testing, and pre-implantation genetic diagnosis. It can help identify individuals who carry a single copy of the mutated HBB gene and are at risk of passing the disorder to their children. Additionally, NGS testing can be used to identify the presence of the HBB gene mutation in embryos created through in vitro fertilization, allowing for the selection of embryos without the mutation for implantation. Overall, NGS genetic testing for the HBB gene in sickle cell anemia can provide valuable information for diagnosis, family planning, and reproductive decision-making. |
