SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test
Cost: AED 4400.0
Overview
The SUCLA2 gene is associated with mitochondrial DNA (mtDNA) depletion syndrome, a rare genetic disorder that affects the mitochondria, the energy-producing structures within cells. Mutations in the SUCLA2 gene can lead to a decrease in the amount of mtDNA, which can result in impaired energy production and dysfunction in various organs and tissues.
Test Details
The SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test is conducted using NGS (Next-Generation Sequencing) technology. NGS genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial DNA depletion syndrome, NGS can be used to identify mutations in the SUCLA2 gene and other relevant genes associated with the disorder.
Test Components and Price
- Components: SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test
- Price: AED 4400.0
Sample Condition
The test can be conducted using blood or extracted DNA. Alternatively, one drop of blood can be collected on an FTA Card.
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Test Type
The test is specifically designed for diagnosing neurological disorders.
Doctor and Test Department
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is undergoing the SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the syndrome.
Importance of Genetic Testing
NGS genetic testing for mitochondrial DNA depletion syndrome can help in diagnosing the condition, determining the underlying genetic cause, and guiding treatment decisions. It can also provide information about the likelihood of passing the condition on to future generations.
It is crucial to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics. They can provide appropriate counseling and guidance based on the test results.
| Test Name | SUCLA2 Gene Mitochondrial DNA depletion syndrome 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 SUCLA2 Gene Mitochondrial DNA depletion syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SUCLA2 Gene Mitochondrial DNA depletion syndrome |
| Test Details |
The SUCLA2 gene is associated with mitochondrial DNA (mtDNA) depletion syndrome, a rare genetic disorder that affects the mitochondria, the energy-producing structures within cells. Mutations in the SUCLA2 gene can lead to a decrease in the amount of mtDNA, which can result in impaired energy production and dysfunction in various organs and tissues. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial DNA depletion syndrome, NGS can be used to identify mutations in the SUCLA2 gene and other relevant genes associated with the disorder. NGS genetic testing for mitochondrial DNA depletion syndrome can help in diagnosing the condition, determining the underlying genetic cause, and guiding treatment decisions. It can also provide information about the likelihood of passing the condition on to future generations. It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics, as they can provide appropriate counseling and guidance based on the test results. |
