Short Description

Usher syndrome is a condition characterized by partial or total sensorineural hearing loss and vision loss that aggravates over time. _x000D_ There are three major types of Usher syndrome namely types I, II and III distinguished by the severity of hearing loss, the presence or absence of balance problems_x000D_ and the age at which signs and symptoms appear. The types are further divided into subtypes based on their genetic cause. Mutations in several different genes on different chromosomes are associated with Usher syndrome. This test is useful for the genetic determination of this disorder.

PreTest Information

Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Detail Description

Nx GEN SEQUENCING: USHER SYNDROME Test cost INR:28665 symptoms diagnosis

Usher syndrome is a genetic condition that affects hearing, vision, and balance. It is caused by mutations in genes that are involved in the development and function of sensory cells in the inner ear and retina. There are three types of Usher syndrome, each with different symptoms and severity.

The symptoms of Usher syndrome can vary depending on the type and severity of the condition. Common symptoms include:

• Hearing loss or deafness
• Difficulty seeing in dimly lit areas
• Tunnel vision or loss of peripheral vision
• Balance problems or vertigo

If you or a loved one is experiencing any of these symptoms, it is important to speak with a healthcare provider. They may recommend genetic testing to determine if Usher syndrome is the cause.

Nx GEN SEQUENCING

Nx GEN SEQUENCING is a genetic testing method that can be used to diagnose Usher syndrome. It is a type of next-generation sequencing that can analyze multiple genes at once, making it a more efficient and cost-effective option than traditional genetic testing methods.

The cost of Nx GEN SEQUENCING for Usher syndrome in India is INR 28,665. This cost may vary depending on the testing facility and any additional fees that may be associated with the testing process.

Diagnosing Usher Syndrome

Diagnosing Usher syndrome typically involves a combination of clinical evaluation, hearing and vision tests, and genetic testing. Nx GEN SEQUENCING can be used to identify mutations in genes that are associated with Usher syndrome, which can help with diagnosis and inform treatment options.

If you or a loved one is experiencing symptoms of Usher syndrome, it is important to speak with a healthcare provider about your options for testing and diagnosis. With early diagnosis and treatment, it is possible to manage the symptoms of Usher syndrome and maintain quality of life.

Conclusion

Usher syndrome is a genetic condition that can cause hearing loss, vision problems, and balance issues. Nx GEN SEQUENCING is a genetic testing method that can be used to diagnose Usher syndrome and identify mutations in genes associated with the condition. The cost of Nx GEN SEQUENCING for Usher syndrome in India is INR 28,665. If you or a loved one is experiencing symptoms of Usher syndrome, it is important to speak with a healthcare provider about your options for testing and diagnosis.

At DNA Labs India, we offer a range of genetic testing services, including Nx GEN SEQUENCING for Usher syndrome. Contact us today to learn more about our testing options and how we can help with your genetic testing needs.

Usher syndrome is a condition characterized by partial or total sensorineural hearing loss and vision loss that aggravates over time. There are three major types of Usher syndrome namely types I, II and III distinguished by the severity of hearing loss, the presence or absence of balance problems and the age at which signs and symptoms appear. The types are further divided into subtypes based on their genetic cause. Mutations in several different genes on different chromosomes are associated with Usher syndrome. This test is useful for the genetic determination of this disorder.