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VDAC1 Gene Encephalopathy mitochondrial Genetic Test

4,400 د.إ

-21%

The VDAC1 Gene Encephalopathy Mitochondrial Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the VDAC1 gene that are associated with mitochondrial encephalopathy, a complex condition characterized by brain dysfunction along with muscle weakness and other systemic symptoms. Mitochondrial encephalopathies are a group of disorders that arise from defects in mitochondrial function, crucial for energy production in cells. The VDAC1 gene plays a significant role in the regulation of mitochondrial membrane potential and apoptosis, making its mutations potentially impactful on cellular energy metabolism and neuronal health.

This test is particularly vital for individuals presenting symptoms of mitochondrial encephalopathy or those with a family history of the condition, as it provides crucial information for diagnosis, management, and treatment planning. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test ensures accuracy and reliability in results. The cost of the VDAC1 Gene Encephalopathy Mitochondrial Genetic Test is 4400 AED, reflecting the sophisticated technology and expertise involved in conducting the analysis and interpreting the results. For patients and families, this test represents a step towards understanding their genetic makeup and managing the implications of mitochondrial diseases with a more targeted approach.

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VDAC1 Gene Encephalopathy Mitochondrial Genetic Test

Cost: 4400.0 AED

Test Components:

  • 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:

Clinical History of Patient who is going for VDAC1 Gene Encephalopathy Mitochondrial NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with VDAC1 Gene Encephalopathy Mitochondrial

Test Details:

The Encephalopathy Mitochondrial NGS Genetic Test is a genetic test that is used to identify mutations in the VDAC1 gene. This gene is responsible for encoding a protein that is found in the mitochondrial outer membrane. Mutations in this gene have been linked to a variety of mitochondrial diseases, including encephalopathy.

Encephalopathy is a condition that affects the brain and can cause a range of symptoms, including seizures, cognitive impairment, and developmental delays. Mitochondrial diseases are caused by mutations in the genes that are responsible for the production of energy in the body. These mutations can lead to a range of symptoms, including muscle weakness, vision and hearing problems, and developmental delays.

NGS (Next Generation Sequencing) is a technique that is used to sequence the DNA of an individual. This technique allows for the identification of mutations in genes that are associated with various diseases, including mitochondrial diseases. The Encephalopathy Mitochondrial NGS Genetic Test uses this technique to identify mutations in the VDAC1 gene that may be responsible for the development of encephalopathy.

Overall, the Encephalopathy Mitochondrial NGS Genetic Test is a useful tool for the diagnosis and management of mitochondrial diseases, including encephalopathy. It can help identify the specific mutations that are responsible for the disease, which can inform treatment decisions and help improve outcomes for patients.

Test Name VDAC1 Gene Encephalopathy mitochondrial 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 VDAC1 Gene Encephalopathy mitochondrial NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with VDAC1 Gene Encephalopathy mitochondrial
Test Details

Encephalopathy mitochondrial NGS Genetic Test is a genetic test that is used to identify mutations in the VDAC1 gene. This gene is responsible for encoding a protein that is found in the mitochondrial outer membrane. Mutations in this gene have been linked to a variety of mitochondrial diseases, including encephalopathy.

Encephalopathy is a condition that affects the brain and can cause a range of symptoms, including seizures, cognitive impairment, and developmental delays. Mitochondrial diseases are caused by mutations in the genes that are responsible for the production of energy in the body. These mutations can lead to a range of symptoms, including muscle weakness, vision and hearing problems, and developmental delays.

NGS (Next Generation Sequencing) is a technique that is used to sequence the DNA of an individual. This technique allows for the identification of mutations in genes that are associated with various diseases, including mitochondrial diseases. The Encephalopathy mitochondrial NGS Genetic Test uses this technique to identify mutations in the VDAC1 gene that may be responsible for the development of encephalopathy.

Overall, the Encephalopathy mitochondrial NGS Genetic Test is a useful tool for the diagnosis and management of mitochondrial diseases, including encephalopathy. It can help identify the specific mutations that are responsible for the disease, which can inform treatment decisions and help improve outcomes for patients.