Parkinson Disease Panel NGS Genetic Test
Test Name: Parkinson Disease Panel NGS Genetic DNA Test
Components 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 Parkinson Disease Panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Parkinson Disease Panel.
Test Details
The Parkinson Disease Panel NGS Genetic DNA Test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze multiple genes associated with Parkinson’s disease. This test is designed to identify genetic mutations or variants that may increase the risk of developing Parkinson’s disease or contribute to the development of the disease in individuals who have already been diagnosed.
The Parkinson Disease Panel NGS Genetic DNA Test typically includes analysis of genes such as SNCA, LRRK2, PARK2, PINK1, and DJ-1, among others. These genes are known to play a role in the development and progression of Parkinson’s disease, and mutations or variants in these genes can increase an individual’s risk of developing the disease.
The test is typically performed on a blood or saliva sample, and results are typically available within a few weeks. If genetic mutations or variants are identified, the results can be used to guide treatment and management strategies for individuals with Parkinson’s disease, as well as to inform genetic counseling and family planning decisions.
Test Name | Parkinson disease panel NGS Genetic DNA 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 Parkinson disease panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Parkinson disease panel |
Test Details | The Parkinson disease panel NGS genetic DNA test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze multiple genes associated with Parkinson’s disease. This test is designed to identify genetic mutations or variants that may increase the risk of developing Parkinson’s disease or contribute to the development of the disease in individuals who have already been diagnosed. The Parkinson disease panel NGS genetic DNA test typically includes analysis of genes such as SNCA, LRRK2, PARK2, PINK1, and DJ-1, among others. These genes are known to play a role in the development and progression of Parkinson’s disease, and mutations or variants in these genes can increase an individual’s risk of developing the disease. The test is typically performed on a blood or saliva sample, and results are typically available within a few weeks. If genetic mutations or variants are identified, the results can be used to guide treatment and management strategies for individuals with Parkinson’s disease, as well as to inform genetic counseling and family planning decisions. |