Short Description

NGS genetic DNA test detecets for variant and mutation detection in NDUFS8 gene for Leigh syndrome

PreTest Information

Clinical History of Patient who is going for NDUFS8 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS8 Gene Leigh syndrome

Detail Description

NDUFS8 Gene Leigh Syndrome NGS Genetic DNA Test Cost INR 20,000: Symptoms and Diagnosis

Leigh syndrome is a rare neurological disorder that affects the central nervous system. It is a progressive condition that typically begins in infancy or early childhood. The symptoms of Leigh syndrome vary, but they often include developmental delays, weakness, and difficulty breathing. There are several different types of Leigh syndrome, each caused by a different genetic mutation.

One of the genes that can cause Leigh syndrome is the NDUFS8 gene. This gene is responsible for producing a protein that is essential for the function of mitochondria, the energy-producing structures within cells. When the NDUFS8 gene is mutated, the mitochondria cannot function properly, leading to the symptoms of Leigh syndrome.

NGS Genetic DNA Test for NDUFS8 Gene Leigh Syndrome

If you or a loved one is experiencing symptoms of Leigh syndrome, it is important to undergo genetic testing to determine the underlying cause of the condition. The NGS (next-generation sequencing) genetic DNA test is a comprehensive test that can detect mutations in the NDUFS8 gene and other genes associated with Leigh syndrome.

The NGS genetic DNA test is a non-invasive test that requires only a small blood sample. The sample is sent to a laboratory for analysis, where it is sequenced to identify any mutations in the NDUFS8 gene and other genes associated with Leigh syndrome. The test results can help doctors diagnose the condition and develop an appropriate treatment plan.

Symptoms of NDUFS8 Gene Leigh Syndrome

The symptoms of NDUFS8 gene Leigh syndrome can vary widely, but they often include:

• Developmental delays
• Weakness
• Difficulty breathing
• Seizures
• Loss of motor control
• Visual and hearing impairment
• Encephalopathy (brain disease)

These symptoms can range from mild to severe and can progress over time. It is important to seek medical attention if you or a loved one is experiencing any of these symptoms.

Diagnosis of NDUFS8 Gene Leigh Syndrome

The diagnosis of NDUFS8 gene Leigh syndrome typically involves a combination of genetic testing, medical history, and physical examination. If a doctor suspects Leigh syndrome, they may order the NGS genetic DNA test to identify any mutations in the NDUFS8 gene or other genes associated with the condition.

Additional tests may also be performed to assess the function of the mitochondria, such as muscle biopsies or imaging studies. A team of medical specialists, including neurologists and genetic counselors, may be involved in the diagnosis and management of Leigh syndrome.

Cost of NGS Genetic DNA Test for NDUFS8 Gene Leigh Syndrome

The cost of the NGS genetic DNA test for NDUFS8 gene Leigh syndrome in India is approximately INR 20,000. This cost may vary depending on the laboratory and location.

Conclusion

NDUFS8 gene Leigh syndrome is a rare neurological disorder that can cause a range of symptoms, including developmental delays, weakness, and difficulty breathing. The NGS genetic DNA test is a comprehensive test that can help diagnose the condition and guide treatment. If you or a loved one is experiencing symptoms of Leigh syndrome, it is important to seek medical attention and undergo genetic testing.

At DNA Labs India, we offer state-of-the-art NGS genetic DNA testing services for a wide range of genetic disorders, including Leigh syndrome caused by the NDUFS8 gene mutation. Contact us today to learn more about our testing services and how we can help you.

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 NDUFS8 Gene Leigh syndrome NGS Genetic DNA Test