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COX6A1 Gene CMTRID Genetic Test

4,400 د.إ

-21%

The COX6A1 gene CMTRID genetic test is a specialized diagnostic tool used to identify mutations in the COX6A1 gene, which can be associated with complex metabolic and neurological disorders. This test is crucial for individuals who may be exhibiting symptoms related to these conditions or have a family history of related genetic disorders. By analyzing the genetic material for specific mutations in the COX6A1 gene, healthcare providers can gain valuable insights into a patient’s condition, enabling them to make more informed decisions regarding treatment and management.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities and commitment to providing accurate and reliable results. The cost of the COX6A1 gene CMTRID genetic test is 4400 AED, an investment that can provide individuals and their families with essential information about their genetic health, potentially guiding therapeutic interventions and lifestyle adjustments to manage or mitigate the impact of the associated conditions.

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  • This test is not intended for medical diagnosis or treatment
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COX6A1 Gene CMTRID Genetic Test

At DNA Labs UAE, we offer the COX6A1 Gene CMTRID Genetic Test for individuals who may be experiencing neurological disorders. This test can help diagnose, provide prognosis, and aid in treatment planning for mitochondrial diseases.

Test Details

The COX6A1 gene is a nuclear gene that encodes a subunit of cytochrome c oxidase, which plays a crucial role in the electron transport chain in mitochondria. Mutations in this gene have been linked to various mitochondrial disorders, such as Leigh syndrome and mitochondrial encephalomyopathy.

Our CMTRID NGS genetic test utilizes next-generation sequencing technology to analyze the entire mitochondrial genome and selected nuclear genes associated with mitochondrial disorders, including the COX6A1 gene. By identifying mutations in these genes, we can determine if they are responsible for mitochondrial disease, allowing for accurate diagnosis, prognosis, and treatment planning.

Components

  • Test Name: COX6A1 Gene CMTRID 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the COX6A1 Gene CMTRID NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by COX6A1 Gene CMTRID. This information helps us gain a comprehensive understanding of the patient’s condition and aids in accurate testing and interpretation of results.

Cost

The cost of the COX6A1 Gene CMTRID Genetic Test is 4400.0 AED.

At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. If you suspect a mitochondrial disorder or have any concerns about your health, we recommend consulting with a neurologist who can guide you through the testing process and assist with diagnosis and treatment planning.

Test Name COX6A1 Gene CMTRID 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 COX6A1 Gene CMTRID NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COX6A1 Gene CMTRID
Test Details

The COX6A1 gene is a nuclear gene that encodes a subunit of cytochrome c oxidase, which is involved in the electron transport chain in mitochondria. Mutations in this gene have been associated with various mitochondrial disorders, including Leigh syndrome and mitochondrial encephalomyopathy.

The CMTRID NGS genetic test is a next-generation sequencing test that analyzes the entire mitochondrial genome and selected nuclear genes that are associated with mitochondrial disorders, including the COX6A1 gene. This test can identify mutations in these genes that may be responsible for mitochondrial disease and can help with diagnosis, prognosis, and treatment planning.