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.