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NDUFAF6 Gene Leigh syndrome Genetic Test

4,400 د.إ

-21%

The NDUFAF6 gene Leigh syndrome genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the NDUFAF6 gene that are associated with Leigh syndrome, a severe neurological disorder. This condition typically emerges in infancy and is characterized by progressive loss of mental and movement abilities, potentially leading to serious health complications. The test is crucial for families seeking answers to unexplained symptoms of neurodegeneration in their children, as early detection can aid in managing the symptoms and improving the quality of life of the affected individual. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately analyze and interpret the genetic information. By opting for this test at DNA Labs UAE, individuals gain access to comprehensive genetic insights, enabling targeted interventions and personalized care plans for those affected by Leigh syndrome.

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NDUFAF6 Gene Leigh Syndrome Genetic Test

Test Name: NDUFAF6 Gene Leigh Syndrome Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for NDUFAF6 Gene Leigh Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF6 Gene Leigh Syndrome.

What is NDUFAF6 Gene Leigh Syndrome Genetic Test?

The NDUFAF6 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive loss of mental and movement abilities, as well as other symptoms such as muscle weakness, poor coordination, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the NDUFAF6 gene for mutations or variations that may be associated with Leigh syndrome. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of the genetic factors contributing to the condition.

By identifying mutations or variations in the NDUFAF6 gene, NGS genetic testing can help in confirming a diagnosis of Leigh syndrome and provide information about the specific genetic cause of the condition. This information can be useful for understanding the underlying mechanisms of the disease and for genetic counseling purposes.

It is important to note that NGS genetic testing for Leigh syndrome may be recommended in individuals who have symptoms suggestive of the condition, as well as in family members of affected individuals who may be at risk of carrying the same genetic mutation. A healthcare professional or genetic counselor can provide more information and guidance regarding the appropriateness and availability of NGS genetic testing for Leigh syndrome.

Test Name NDUFAF6 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 NDUFAF6 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF6 Gene Leigh syndrome
Test Details

The NDUFAF6 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive loss of mental and movement abilities, as well as other symptoms such as muscle weakness, poor coordination, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the NDUFAF6 gene for mutations or variations that may be associated with Leigh syndrome. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of the genetic factors contributing to the condition.

By identifying mutations or variations in the NDUFAF6 gene, NGS genetic testing can help in confirming a diagnosis of Leigh syndrome and provide information about the specific genetic cause of the condition. This information can be useful for understanding the underlying mechanisms of the disease and for genetic counseling purposes.

It is important to note that NGS genetic testing for Leigh syndrome may be recommended in individuals who have symptoms suggestive of the condition, as well as in family members of affected individuals who may be at risk of carrying the same genetic mutation. A healthcare professional or genetic counselor can provide more information and guidance regarding the appropriateness and availability of NGS genetic testing for Leigh syndrome.