BOLA3 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 2 Genetic Test
Are you looking for a genetic test to diagnose Multiple Mitochondrial Dysfunctions Syndrome Type 2 (MMDS2)? DNA Labs UAE offers the BOLA3 gene multiple mitochondrial dysfunctions syndrome type 2 genetic test. This test analyzes the BOLA3 gene to identify mutations or variations that may be causing the disorder.
Test Components
The BOLA3 gene multiple mitochondrial dysfunctions syndrome type 2 genetic test includes:
- 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre-Test Information
Before undergoing the BOLA3 gene multiple mitochondrial dysfunctions syndrome type 2 genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with MMDS2.
About MMDS2
Multiple Mitochondrial Dysfunctions Syndrome Type 2 (MMDS2) is a genetic disorder that affects the function of mitochondria, which are responsible for producing energy in cells. The BOLA3 gene is associated with this condition. By analyzing the patient’s DNA, the NGS genetic testing method can identify mutations or variations in the BOLA3 gene that may be causing MMDS2.
Diagnosing MMDS2 through the BOLA3 gene multiple mitochondrial dysfunctions syndrome type 2 genetic test can provide valuable information for determining appropriate treatment options and understanding the potential risks of the condition.
Don’t wait any longer. Get the answers you need with the BOLA3 gene multiple mitochondrial dysfunctions syndrome type 2 genetic test offered by DNA Labs UAE. Contact us today to schedule your test.
Test Name | BOLA3 Gene Multiple mitochondrial dysfunctions syndrome type 2 Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for BOLA3 Gene Multiple mitochondrial dysfunctions syndrome type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with BOLA3 Gene Multiple mitochondrial dysfunctions syndrome type 2 |
Test Details |
The BOLA3 gene is associated with a condition called Multiple Mitochondrial Dysfunctions Syndrome Type 2 (MMDS2). This genetic disorder affects the function of mitochondria, which are responsible for producing energy in cells. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of MMDS2, NGS genetic testing can identify mutations or variations in the BOLA3 gene that may be causing the disorder. By analyzing the patient’s DNA, NGS genetic testing can provide valuable information about the presence of BOLA3 gene mutations and help diagnose MMDS2. This information can be crucial for determining appropriate treatment options and understanding the potential risks of the condition. |