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BOLA3 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 2 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The BOLA3 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 2 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect mutations in the BOLA3 gene. These mutations are known to cause Multiple Mitochondrial Dysfunctions Syndrome Type 2 (MMDS2), a rare genetic disorder characterized by a wide range of clinical symptoms, including severe metabolic abnormalities, developmental delay, and lactic acidosis. The condition stems from impaired function of the mitochondrial respiratory chain, crucial for energy production in cells.

The test is conducted using a sample of the patient’s blood or saliva, from which DNA is extracted and analyzed for specific genetic alterations in the BOLA3 gene. This precise approach enables healthcare providers to make an accurate diagnosis, essential for managing the condition effectively.

Priced at 4400 AED, the test is a significant investment in understanding and addressing this complex disorder. Conducted at the state-of-the-art facilities of DNA Labs UAE, patients can expect a high standard of accuracy and reliability in their test results, providing essential information for the management of MMDS2. This genetic test is a crucial tool for families seeking answers to unexplained symptoms related to mitochondrial dysfunction, offering a pathway towards tailored treatment and management plans.

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  • This test is not intended for medical diagnosis or treatment
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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.