PDSS1 Gene Coenzyme Q10 Deficiency Type 2 Genetic Test
Components: PDSS1 Gene Coenzyme Q10 deficiency type 2 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: Clinical History of Patient who is going for PDSS1 Gene Coenzyme Q10 deficiency type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PDSS1 Gene Coenzyme Q10 deficiency type 2.
Test Details:
The PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is a diagnostic test that analyzes the PDSS1 gene for mutations that can lead to coenzyme Q10 deficiency type 2. This test uses next-generation sequencing (NGS) technology to examine the entire coding region of the PDSS1 gene, which is responsible for producing an enzyme necessary for the production of coenzyme Q10.
Coenzyme Q10 is an essential molecule that plays a vital role in the production of energy within cells. Deficiency of coenzyme Q10 can lead to a wide range of symptoms, including muscle weakness, seizures, developmental delays, and heart problems.
The PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is used to diagnose individuals who exhibit symptoms of coenzyme Q10 deficiency. It is also used to identify individuals who may be carriers of the mutation and are at risk of passing it on to their children. The test involves collecting a blood sample from the individual and analyzing the DNA for mutations in the PDSS1 gene.
Results are typically available within a few weeks and can help guide treatment and management of the condition. Overall, the PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is a valuable tool for diagnosing and managing coenzyme Q10 deficiency, which can have significant impacts on an individual’s health and quality of life.
| Test Name | PDSS1 Gene Coenzyme Q10 deficiency 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 PDSS1 Gene Coenzyme Q10 deficiency type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PDSS1 Gene Coenzyme Q10 deficiency type 2 |
| Test Details |
PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is a diagnostic test that analyzes the PDSS1 gene for mutations that can lead to coenzyme Q10 deficiency type 2. This test uses next-generation sequencing (NGS) technology to examine the entire coding region of the PDSS1 gene, which is responsible for producing an enzyme necessary for the production of coenzyme Q10. Coenzyme Q10 is an essential molecule that plays a vital role in the production of energy within cells. Deficiency of coenzyme Q10 can lead to a wide range of symptoms, including muscle weakness, seizures, developmental delays, and heart problems. The PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is used to diagnose individuals who exhibit symptoms of coenzyme Q10 deficiency. It is also used to identify individuals who may be carriers of the mutation and are at risk of passing it on to their children. The test involves collecting a blood sample from the individual and analyzing the DNA for mutations in the PDSS1 gene. Results are typically available within a few weeks and can help guide treatment and management of the condition. Overall, the PDSS1 gene coenzyme Q10 deficiency type 2 NGS genetic test is a valuable tool for diagnosing and managing coenzyme Q10 deficiency, which can have significant impacts on an individual’s health and quality of life. |
