Short Description

NGS genetic DNA test detecets for variant and mutation detection in MT-ND6 gene for Leigh syndrome due to mitochondrial complex I deficiency

PreTest Information

Clinical History of Patient who is going for MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency

Detail Description

MT-ND6 Gene Leigh Syndrome: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Leigh syndrome is a rare genetic disorder that affects the central nervous system. It is usually caused by a deficiency in mitochondrial complex I, which is involved in energy production in cells. One of the genes associated with Leigh syndrome is the MT-ND6 gene. In this blog post, we will discuss the symptoms of Leigh syndrome due to mitochondrial complex I deficiency, the diagnosis process, and the cost of NGS genetic DNA testing for the MT-ND6 gene in India.

Symptoms of Leigh Syndrome Due to Mitochondrial Complex I Deficiency

The symptoms of Leigh syndrome can vary widely from person to person. However, some of the most common symptoms include:

• Developmental delays
• Weakness or loss of muscle tone
• Poor growth
• Seizures
• Difficulty swallowing
• Vomiting
• Respiratory problems
• Loss of vision or hearing
• Abnormal eye movements

These symptoms usually appear in the first year of life, but they can also appear later in childhood or even adulthood. In some cases, the symptoms may worsen over time, leading to severe disability or even death.

Diagnosis of Leigh Syndrome Due to Mitochondrial Complex I Deficiency

Diagnosing Leigh syndrome can be challenging because the symptoms can be similar to those of other neurological disorders. However, there are several diagnostic tests that can help confirm a diagnosis of Leigh syndrome due to mitochondrial complex I deficiency.

One of the most common tests is a brain MRI, which can show characteristic changes in the brain associated with Leigh syndrome. Genetic testing can also be done to identify mutations in the genes associated with Leigh syndrome, such as the MT-ND6 gene.

NGS Genetic DNA Test Cost for MT-ND6 Gene in India

The cost of NGS genetic DNA testing for the MT-ND6 gene in India can vary depending on the laboratory and the specific test being done. However, on average, the cost of this test is around INR 20,000.

NGS genetic DNA testing is a powerful tool for diagnosing genetic disorders like Leigh syndrome due to mitochondrial complex I deficiency. This type of testing can identify mutations in specific genes, such as the MT-ND6 gene, that are associated with the disorder. This can help doctors make an accurate diagnosis and develop an appropriate treatment plan.

Conclusion

Leigh syndrome due to mitochondrial complex I deficiency is a rare genetic disorder that can cause a wide range of symptoms. Diagnosis can be challenging, but with the help of diagnostic tests like brain MRI and genetic testing, doctors can confirm a diagnosis and develop an appropriate treatment plan. NGS genetic DNA testing for the MT-ND6 gene is an important tool for diagnosing Leigh syndrome and can be done at a cost of around INR 20,000 in India.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA testing for the MT-ND6 gene. If you suspect that you or a loved one may have Leigh syndrome due to mitochondrial complex I deficiency, contact us today to learn more about our testing services.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for MT-ND6 Gene Leigh syndrome due to mitochondrial complex I deficiency NGS Genetic DNA Test