APOB Gene Hypobetalipoproteinemia type 1 Genetic Test
At DNA Labs UAE, we offer the APOB Gene Hypobetalipoproteinemia type 1 Genetic Test at a cost of 4400.0 AED. This test is used to diagnose and identify genetic variations in the APOB gene, which is responsible for producing the apoB protein that plays a crucial role in the transportation of fats and cholesterol in the body.
Test Components and Details
- Test Name: APOB Gene Hypobetalipoproteinemia type 1 Genetic Test
- 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
- Pre Test Information: Clinical History of Patient who is going for APOB Gene Hypobetalipoproteinemia type 1 NGS Genetic DNA Test, Genetic Counselling session to draw a pedigree chart of family members affected with Hypobetalipoproteinemia type 1
About Hypobetalipoproteinemia type 1
Hypobetalipoproteinemia type 1 is a rare genetic disorder caused by mutations in the APOB gene. These mutations result in the production of abnormal or nonfunctional apoB protein, leading to very low levels of low-density lipoprotein (LDL) cholesterol and triglycerides in the blood.
NGS Technology for Genetic Testing
NGS (Next-Generation Sequencing) genetic testing is a powerful and advanced technique used to analyze multiple genes simultaneously. In the context of APOB gene hypobetalipoproteinemia type 1, NGS genetic testing can identify specific mutations or variations in the APOB gene that are responsible for the disorder. This testing method allows for a comprehensive analysis of the entire gene, providing a more accurate and detailed understanding of the genetic variations present.
Benefits of APOB Gene Hypobetalipoproteinemia type 1 Genetic Test
NGS genetic testing for APOB gene hypobetalipoproteinemia type 1 can be beneficial in several ways:
- Diagnosis: The test helps in diagnosing the disorder accurately.
- Genetic Counseling: It aids in providing information and guidance to individuals and families affected by the disorder.
- Treatment Decisions: The test results can potentially guide treatment decisions for individuals with hypobetalipoproteinemia type 1.
- Carrier Testing: The test can be used for carrier testing in individuals with a family history of the disorder.
It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations.
| Test Name | APOB Gene Hypobetalipoproteinemia type 1 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for APOB Gene Hypobetalipoproteinemia type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypobetalipoproteinemia type 1 |
| Test Details |
The APOB gene is responsible for providing instructions for making a protein called apolipoprotein B (apoB). This protein plays a crucial role in the transportation of fats and cholesterol in the body. Hypobetalipoproteinemia type 1 is a rare genetic disorder caused by mutations in the APOB gene. These mutations lead to the production of abnormal or nonfunctional apoB protein. As a result, individuals with this condition have very low levels of low-density lipoprotein (LDL) cholesterol and triglycerides in their blood. NGS (Next-Generation Sequencing) genetic testing is a powerful and advanced technique used to analyze multiple genes simultaneously. In the context of APOB gene hypobetalipoproteinemia type 1, NGS genetic testing can identify specific mutations or variations in the APOB gene that are responsible for the disorder. This testing method allows for a comprehensive analysis of the entire gene, providing a more accurate and detailed understanding of the genetic variations present. NGS genetic testing for APOB gene hypobetalipoproteinemia type 1 can help with diagnosis, genetic counseling, and potentially guide treatment decisions. It can also be used for carrier testing in individuals with a family history of the disorder. It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations. |
