Short Description

NGS genetic DNA test detecets for variant and mutation detection in TMPRSS3 gene for Deafness, autosomal recessive type 8/10

PreTest Information

Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN33

Detail Description

TMPRSS3 Gene Deafness: Understanding Autosomal Recessive Type 8/10 NGS Genetic DNA Test

Deafness is a condition that affects millions of people worldwide. It can be caused by a variety of factors, including genetic mutations. One such mutation is found in the TMPRSS3 gene, which is responsible for autosomal recessive type 8/10 deafness. Understanding this condition and the NGS Genetic DNA Test that can detect it is important for individuals and families affected by deafness.

Symptoms of Autosomal Recessive Type 8/10 Deafness

Autosomal recessive type 8/10 deafness is characterized by profound hearing loss that is present from birth. Individuals with this condition may have difficulty hearing sounds that are at a normal volume for others. They may also have difficulty understanding speech, particularly in noisy environments. Some individuals may experience tinnitus, or ringing in the ears. In some cases, the symptoms of this condition may be mild, while in others they may be more severe.

Diagnosis of Autosomal Recessive Type 8/10 Deafness

If you or a loved one is experiencing symptoms of hearing loss, it is important to see a healthcare provider for an evaluation. Your healthcare provider may refer you to a specialist, such as an audiologist or genetic counselor, for further testing. The NGS Genetic DNA Test is a powerful tool that can detect mutations in the TMPRSS3 gene that are associated with autosomal recessive type 8/10 deafness.

NGS Genetic DNA Test for Autosomal Recessive Type 8/10 Deafness

The NGS Genetic DNA Test is a non-invasive test that involves collecting a sample of DNA from the individual being tested. This can be done through a simple cheek swab or blood sample. The sample is then analyzed in a laboratory using next-generation sequencing technology. This technology allows for the detection of mutations in the TMPRSS3 gene that are associated with autosomal recessive type 8/10 deafness.

Cost of NGS Genetic DNA Test for Autosomal Recessive Type 8/10 Deafness

The cost of the NGS Genetic DNA Test for autosomal recessive type 8/10 deafness varies depending on the provider. At DNA Labs India, the cost of this test is INR 20,000. This includes the cost of sample collection, DNA analysis, and interpretation of results by a certified genetic counselor.

Conclusion

Autosomal recessive type 8/10 deafness is a genetic condition that can have a profound impact on an individual's quality of life. Understanding the symptoms and diagnosis of this condition is important for early detection and intervention. The NGS Genetic DNA Test is a powerful tool that can detect mutations in the TMPRSS3 gene that are associated with this condition. If you or a loved one is experiencing symptoms of hearing loss, consider getting tested to determine if autosomal recessive type 8/10 deafness is the cause.

At DNA Labs India, we are dedicated to providing accurate, reliable genetic testing services to individuals and families. Contact us today to learn more about our NGS Genetic DNA Test for autosomal recessive type 8/10 deafness.

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 TMPRSS3 Gene Deafness, autosomal recessive type 8/10 NGS Genetic DNA Test