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COQ2 Gene Coenzyme Q10 Deficiency Type 1 Genetic Test

4,400 د.إ

-21%

The COQ2 gene plays a critical role in the body by contributing to the production of Coenzyme Q10 (CoQ10), a substance essential for the proper functioning of cells and the generation of energy within the mitochondria. Mutations in the COQ2 gene can lead to Coenzyme Q10 deficiency type 1, a condition that affects various systems of the body and can lead to symptoms such as muscle weakness, seizures, and neurological impairments.

To diagnose this genetic condition, a specific genetic test can be performed that analyzes the COQ2 gene for mutations. This test is crucial for confirming the diagnosis of Coenzyme Q10 deficiency type 1, allowing for appropriate treatment and management strategies to be implemented. Treatment often involves supplementation with CoQ10, which can help alleviate some of the symptoms associated with the deficiency.

In the United Arab Emirates, DNA Labs UAE offers the COQ2 Gene Coenzyme Q10 Deficiency Type 1 Genetic Test. The cost of the test is 4400 AED. DNA Labs UAE is known for its state-of-the-art facilities and expert team of geneticists and medical professionals who ensure accurate and reliable test results. Opting for this test at DNA Labs UAE can provide individuals and families with crucial information regarding the presence of COQ2 gene mutations, guiding healthcare decisions and improving patient outcomes.

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COQ2 Gene Coenzyme Q10 Deficiency Type 1 Genetic Test

Are you or a loved one experiencing symptoms of Coenzyme Q10 deficiency type 1? DNA Labs UAE offers a comprehensive genetic test that can help diagnose this rare genetic disorder. Read on to learn more about the test, its components, cost, symptoms, diagnosis, and more.

Test Name: COQ2 Gene Coenzyme Q10 Deficiency Type 1 Genetic Test

Components: This test analyzes the COQ2 gene responsible for producing an enzyme called para-hydroxybenzoate-polyprenyl transferase, essential for Coenzyme Q10 (CoQ10) biosynthesis.

Price: 4400.0 AED

Sample Condition:

You can provide a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery:

Your test results will be delivered within 3 to 4 weeks.

Method:

We utilize NGS (Next-Generation Sequencing) technology for this genetic test.

Test Type:

This test focuses on neurological disorders.

Doctor:

A neurologist will oversee the testing process.

Test Department:

This test is conducted in our Genetics department.

Pre Test Information:

Prior to the test, we recommend providing the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Coenzyme Q10 deficiency type 1.

Test Details:

The COQ2 gene is responsible for producing the enzyme para-hydroxybenzoate-polyprenyl transferase, necessary for Coenzyme Q10 (CoQ10) biosynthesis. CoQ10 is a vital molecule that plays a crucial role in ATP (adenosine triphosphate) production, the primary source of energy in cells. Mutations in the COQ2 gene can result in CoQ10 deficiency type 1, a rare genetic disorder affecting CoQ10 production.

Our NGS genetic test utilizes advanced sequencing technologies to analyze the entire DNA sequence of the COQ2 gene. This enables the detection of even small changes in the genetic code that may cause CoQ10 deficiency. The test can help diagnose CoQ10 deficiency type 1 and provide valuable information for genetic counseling and family planning.

Furthermore, the test results can assist healthcare providers in developing personalized treatment plans for individuals with CoQ10 deficiency. These plans may include CoQ10 supplementation and lifestyle modifications.

Test Name COQ2 Gene Coenzyme Q10 deficiency type 1 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 COQ2 Gene Coenzyme Q10 deficiency type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COQ2 Gene Coenzyme Q10 deficiency type 1
Test Details

The COQ2 gene is responsible for producing an enzyme called para-hydroxybenzoate-polyprenyl transferase, which is essential for the biosynthesis of Coenzyme Q10 (CoQ10). CoQ10 is a vital molecule that plays a crucial role in the production of ATP (adenosine triphosphate), the primary source of energy in cells. Mutations in the COQ2 gene can lead to CoQ10 deficiency type 1, a rare genetic disorder that affects the production of CoQ10.

NGS (Next-Generation Sequencing) genetic testing is a powerful diagnostic tool that can identify mutations in the COQ2 gene. This test uses advanced sequencing technologies to analyze the entire DNA sequence of the gene, enabling the detection of even small changes in the genetic code that may cause CoQ10 deficiency.

The NGS genetic test for COQ2 gene mutations can help diagnose CoQ10 deficiency type 1 and provide valuable information for genetic counseling and family planning. It can also help healthcare providers develop personalized treatment plans for individuals with CoQ10 deficiency, such as CoQ10 supplementation and lifestyle modifications.