Short Description

NGS genetic DNA test detecets for variant and mutation detection in COX15 gene for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2

PreTest Information

Clinical History of Patient who is going for COX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COX15 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency type 2 NGS Genetic DNA Test gene COX15

Detail Description

COX15 Gene Cardioencephalomyopathy: Understanding Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

COX15 Gene Cardioencephalomyopathy is a rare genetic disorder that affects infants and young children. It is a fatal condition that is characterized by cytochrome c oxidase deficiency type 2. This deficiency leads to a range of symptoms, including neurological impairment, muscle weakness, and respiratory failure. In this blog, we will discuss the symptoms, diagnosis, and NGS genetic DNA test cost for COX15 Gene Cardioencephalomyopathy.

Symptoms of COX15 Gene Cardioencephalomyopathy

The symptoms of COX15 Gene Cardioencephalomyopathy are similar to those of other mitochondrial diseases. The most common symptoms include:

• Developmental delays
• Seizures
• Weakness in the muscles
• Difficulty in feeding
• Respiratory failure
• Neurological impairment
• Cardiomyopathy

These symptoms can vary in severity and may develop at different stages of the disease. In most cases, the symptoms start to appear in infancy or early childhood.

Diagnosis of COX15 Gene Cardioencephalomyopathy

COX15 Gene Cardioencephalomyopathy is diagnosed through genetic testing. The most common test used for diagnosis is the Next-Generation Sequencing (NGS) genetic DNA test. This test identifies mutations in the COX15 gene that are associated with the disease.

The NGS genetic DNA test is a highly sensitive and specific test that can detect mutations in the COX15 gene with a high degree of accuracy. The test is performed on a blood or saliva sample and can be done at any age.

NGS Genetic DNA Test Cost for COX15 Gene Cardioencephalomyopathy

The NGS genetic DNA test for COX15 Gene Cardioencephalomyopathy costs around INR 20,000. This cost may vary depending on the testing laboratory and the location of the patient.

It is important to note that the cost of genetic testing may not be covered by insurance. Patients should check with their insurance provider to determine if the test is covered under their plan.

Conclusion

COX15 Gene Cardioencephalomyopathy is a rare genetic disorder that can be fatal if left untreated. The symptoms of the disease can vary in severity and may develop at different stages of the disease. The NGS genetic DNA test is the most common test used for diagnosis and costs around INR 20,000. Patients should consult with a genetic counselor or a healthcare professional for more information on genetic testing and treatment options.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA testing for COX15 Gene Cardioencephalomyopathy. Contact us today to learn more about our services and how we can help you.