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NDUFA9 Gene Leigh syndrome Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The NDUFA9 gene is associated with a rare genetic disorder known as Leigh syndrome, a severe neurological condition that typically emerges in the first year of life. Leigh syndrome is characterized by progressive loss of mental and movement abilities, leading to early mortality. The condition results from defects in mitochondrial function, where the NDUFA9 gene plays a crucial role in the assembly and function of the mitochondrial complex I, essential for cellular energy production.

In an effort to diagnose and manage Leigh syndrome effectively, genetic testing for mutations in the NDUFA9 gene has become available. DNA Labs UAE offers a comprehensive genetic test specifically designed to detect mutations in the NDUFA9 gene that are linked to Leigh syndrome. This test is a vital tool for families seeking answers to unexplained neurological symptoms in their children, providing crucial information that can guide treatment and management decisions.

The cost of the NDUFA9 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. The test is performed with a high level of accuracy, using advanced genomic technologies to ensure reliable results. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any mutations in the NDUFA9 gene.

For families facing the challenges of Leigh syndrome, the NDUFA9 genetic test offers hope for a clearer understanding of the condition, enabling targeted interventions and support to improve the quality of life for affected individuals.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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NDUFA9 Gene Leigh Syndrome Genetic Test

Test Name: NDUFA9 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

Method: NGS Technology

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for NDUFA9 Gene Leigh Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA9 Gene Leigh Syndrome.

Test Details

The NDUFA9 gene is associated with Leigh syndrome, a rare genetic disorder that primarily affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including developmental delays, muscle weakness, movement disorders, and respiratory problems.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes. In the context of Leigh syndrome, NGS can be used to identify mutations in the NDUFA9 gene and other genes known to be associated with the condition. This type of genetic testing can help confirm a diagnosis, provide information about disease prognosis, and inform reproductive decisions.

If you suspect that you or your child may have Leigh syndrome or have a family history of the condition, it is recommended to consult with a healthcare professional or a genetic counselor who can provide guidance on appropriate genetic testing options, including NGS.

Test Name NDUFA9 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 NDUFA9 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA9 Gene Leigh syndrome
Test Details

The NDUFA9 gene is associated with Leigh syndrome, a rare genetic disorder that primarily affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including developmental delays, muscle weakness, movement disorders, and respiratory problems.

Next-generation sequencing (NGS) is a genetic testing method that allows for the simultaneous analysis of multiple genes. In the context of Leigh syndrome, NGS can be used to identify mutations in the NDUFA9 gene and other genes known to be associated with the condition. This type of genetic testing can help confirm a diagnosis, provide information about disease prognosis, and inform reproductive decisions.

If you suspect that you or your child may have Leigh syndrome or have a family history of the condition, it is recommended to consult with a healthcare professional or a genetic counselor who can provide guidance on appropriate genetic testing options, including NGS.