NDUFAF3 Gene Leigh Syndrome Genetic Test
Are you or a loved one experiencing symptoms of Leigh syndrome? DNA Labs UAE offers the NDUFAF3 Gene Leigh Syndrome Genetic Test to provide you with a comprehensive analysis of your genes and help guide treatment options.
Test Components and Price
The NDUFAF3 Gene Leigh Syndrome Genetic Test is priced at AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously.
Test Type and Doctor
The NDUFAF3 Gene Leigh Syndrome Genetic Test falls under the category of neurological disorders. It is recommended to consult with a neurologist for this test.
Test Department and Pre Test Information
The NDUFAF3 Gene Leigh Syndrome Genetic Test is conducted in the Genetics department. Prior to the test, it is important to provide the clinical history of the patient. A genetic counseling session may also be conducted to draw a pedigree chart of family members affected by NDUFAF3 Gene Leigh syndrome.
Understanding Leigh Syndrome and NGS Genetic Testing
Leigh syndrome is a rare genetic disorder that affects the central nervous system. It is characterized by progressive neurological deterioration, resulting in symptoms such as developmental delay, loss of motor skills, muscle weakness, and respiratory problems.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS can identify mutations or variations in the NDUFAF3 gene that may be causing the disorder. This comprehensive analysis allows for a more accurate diagnosis and can potentially guide treatment options.
Confirming the Presence of Mutations
If a person is suspected of having Leigh syndrome, NGS genetic testing can be recommended by a healthcare professional to confirm the presence of mutations in the NDUFAF3 gene. This information is crucial in understanding the cause of the disease and can provide valuable insights for genetic counseling and family planning.
Don’t wait any longer. Take control of your health and get tested for NDUFAF3 Gene Leigh Syndrome at DNA Labs UAE today.
| Test Name | NDUFAF3 Gene Leigh 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 NDUFAF3 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF3 Gene Leigh syndrome |
| Test Details | The NDUFAF3 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, which can lead to symptoms such as developmental delay, loss of motor skills, muscle weakness, and respiratory problems. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the case of Leigh syndrome, NGS can be used to identify mutations or variations in the NDUFAF3 gene that may be causing the disorder. This type of testing can provide a comprehensive analysis of the gene, allowing for a more accurate diagnosis and potentially guiding treatment options. If a person is suspected of having Leigh syndrome, NGS genetic testing can be recommended by a healthcare professional to confirm the presence of mutations in the NDUFAF3 gene. This can help in understanding the cause of the disease and provide valuable information for genetic counseling and family planning. |
