NDUFA10 Gene Leigh Syndrome Genetic Test
Introduction
The NDUFA10 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. This blog will provide detailed information about the NDUFA10 Gene Leigh Syndrome Genetic Test offered by DNA Labs UAE.
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
Prior to undergoing the NDUFA10 Gene Leigh Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with NDUFA10 Gene Leigh Syndrome.
Test Details
Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems. The NDUFA10 gene is associated with this syndrome.
The NDUFA10 Gene Leigh Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This type of genetic testing allows for the simultaneous analysis of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. By analyzing the NDUFA10 gene, this test can identify mutations or variations that may be associated with Leigh syndrome.
In addition to diagnosing Leigh syndrome, this genetic test can also be used for carrier testing, prenatal testing, and family planning purposes.
It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor. These professionals can interpret the test results and provide appropriate recommendations and support.
Test Name | NDUFA10 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 NDUFA10 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA10 Gene Leigh syndrome |
Test Details | The NDUFA10 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. NGS testing can be used to identify mutations or variations in the NDUFA10 gene that may be associated with Leigh syndrome. The NGS genetic test for NDUFA10 gene mutations can help in diagnosing Leigh syndrome and determining the underlying cause of the condition. It can also be used for carrier testing, prenatal testing, and family planning purposes. It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can interpret the results and provide appropriate recommendations and support. |