Short Description

NGS genetic DNA test detecets for variant and mutation detection in MT-RNR1 gene for Deafness, nonsyndromic, sensorineural, mitochondrial

PreTest Information

Clinical History of Patient who is going for CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER13

Detail Description

MT-RNR1 Gene Deafness - Symptoms, Diagnosis and NGS Genetic DNA Test Cost

MT-RNR1 Gene Deafness is a type of nonsyndromic, sensorineural, mitochondrial deafness that is caused by mutations in the mitochondrial DNA. This type of deafness affects the hair cells in the inner ear, which are responsible for converting sound waves into electrical signals that are sent to the brain.

The symptoms of MT-RNR1 Gene Deafness can vary from person to person, but typically include hearing loss that begins in early childhood or adolescence. The hearing loss is usually bilateral and progressive, meaning that it gets worse over time. In some cases, there may also be tinnitus (ringing in the ears), vertigo (dizziness), and difficulty with balance.

Diagnosing MT-RNR1 Gene Deafness typically involves a thorough medical history and physical exam, as well as a hearing test. Genetic testing may also be recommended to confirm the diagnosis and identify the specific genetic mutation causing the deafness.

NGS (Next Generation Sequencing) Genetic DNA testing is a highly accurate and reliable method of identifying genetic mutations associated with MT-RNR1 Gene Deafness. This type of testing uses advanced sequencing technology to analyze the patient's DNA and identify mutations in the MT-RNR1 gene.

The cost of NGS Genetic DNA testing for MT-RNR1 Gene Deafness in India typically ranges from INR 15,000 to INR 20,000, depending on the specific testing laboratory and the complexity of the test. Some insurance plans may cover the cost of genetic testing, so it is important to check with your insurance provider to determine coverage.

If you or someone you know is experiencing symptoms of MT-RNR1 Gene Deafness, it is important to seek medical attention and undergo appropriate testing to confirm the diagnosis and develop a treatment plan. With early diagnosis and intervention, individuals with MT-RNR1 Gene Deafness can lead healthy, fulfilling lives.

At DNA Labs India, we offer comprehensive genetic testing services for a wide range of genetic conditions, including MT-RNR1 Gene Deafness. Our team of experienced genetic counselors and scientists uses the latest technology and techniques to provide accurate and reliable genetic testing results. Contact us today to learn more about our services and how we can help you.

Key Takeaways

• MT-RNR1 Gene Deafness is a type of nonsyndromic, sensorineural, mitochondrial deafness that is caused by mutations in the mitochondrial DNA.
• The symptoms of MT-RNR1 Gene Deafness typically include hearing loss that begins in early childhood or adolescence, tinnitus, vertigo, and difficulty with balance.
• Diagnosing MT-RNR1 Gene Deafness typically involves a thorough medical history and physical exam, as well as a hearing test and genetic testing.
• NGS Genetic DNA testing is a highly accurate and reliable method of identifying genetic mutations associated with MT-RNR1 Gene Deafness.
• The cost of NGS Genetic DNA testing for MT-RNR1 Gene Deafness in India typically ranges from INR 15,000 to INR 20,000.

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-RNR1 Gene Deafness, nonsyndromic, sensorineural, mitochondrial NGS Genetic DNA Test