SDHA Gene Leigh Syndrome Genetic Test
Components: SDHA Gene Leigh syndrome 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 SDHA Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Leigh syndrome.
Test Details
The SDHA gene Leigh syndrome NGS genetic test is a type of genetic testing that focuses on the SDHA gene and its association with Leigh syndrome. Leigh syndrome is a rare inherited neurological disorder that typically begins in infancy or early childhood and is characterized by progressive loss of motor skills and cognitive decline.
The SDHA gene encodes a subunit of the succinate dehydrogenase enzyme complex, which is involved in the cellular energy production process. Mutations in the SDHA gene can disrupt the normal function of this enzyme complex, leading to the development of Leigh syndrome.
The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the simultaneous analysis of multiple genes, including the SDHA gene, to identify any disease-causing mutations or variants. This method provides a more comprehensive and efficient approach to genetic testing compared to traditional sequencing methods.
The SDHA gene Leigh syndrome NGS genetic test can be used for diagnostic purposes in individuals suspected to have Leigh syndrome or for carrier testing in individuals with a family history of the condition. It can also be utilized for prenatal testing in families with a known SDHA gene mutation.
The results of this genetic test can help in confirming a diagnosis, guiding treatment decisions, providing information on disease prognosis, and informing reproductive planning for affected individuals and their families.
It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetics.
Test Name | SDHA 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 SDHA Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SDHA Gene Leigh syndrome |
Test Details | SDHA gene Leigh syndrome NGS genetic test is a type of genetic testing that focuses on the SDHA gene and its association with Leigh syndrome. Leigh syndrome is a rare inherited neurological disorder that typically begins in infancy or early childhood and is characterized by progressive loss of motor skills and cognitive decline. The SDHA gene encodes a subunit of the succinate dehydrogenase enzyme complex, which is involved in the cellular energy production process. Mutations in the SDHA gene can disrupt the normal function of this enzyme complex, leading to the development of Leigh syndrome. The NGS (Next-Generation Sequencing) technique used in this genetic test allows for the simultaneous analysis of multiple genes, including the SDHA gene, to identify any disease-causing mutations or variants. This method provides a more comprehensive and efficient approach to genetic testing compared to traditional sequencing methods. The SDHA gene Leigh syndrome NGS genetic test can be used for diagnostic purposes in individuals suspected to have Leigh syndrome or for carrier testing in individuals with a family history of the condition. It can also be utilized for prenatal testing in families with a known SDHA gene mutation. The results of this genetic test can help in confirming a diagnosis, guiding treatment decisions, providing information on disease prognosis, and informing reproductive planning for affected individuals and their families. It is important to note that genetic testing should be conducted and interpreted by qualified healthcare professionals with expertise in genetics. |