Short Description

Retinoblastoma is a rare type of eye cancer that usually develops in retina during early childhood typically before the age of 5 years. Hereditary Retinoblastoma is mainly caused by a mutation in a RB1 gene that controls cell division. 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: HEREDITARY RETINOBLASTOMA Test

Retinoblastoma is a rare form of cancer that develops in the retina of the eye. It usually occurs in young children and can lead to vision loss or blindness if not treated promptly. Hereditary retinoblastoma is caused by mutations in the RB1 gene, which is responsible for regulating cell growth and division in the retina.

Symptoms of Hereditary Retinoblastoma

The symptoms of hereditary retinoblastoma can vary depending on the severity of the condition. Some common symptoms include:

• White pupils
• Crossed eyes
• Redness or swelling in the eye
• Eye pain or discomfort

If you notice any of these symptoms in your child, it is important to schedule an appointment with an ophthalmologist as soon as possible.

Diagnosis of Hereditary Retinoblastoma

Diagnosing hereditary retinoblastoma typically involves a comprehensive eye exam, including a dilated retinal exam. Your doctor may also order additional tests, such as:

• Ultrasound
• MRI
• CT scan

If hereditary retinoblastoma is suspected, genetic testing may also be recommended to confirm the diagnosis and identify any mutations in the RB1 gene.

Nx GEN SEQUENCING Test for Hereditary Retinoblastoma

Nx GEN SEQUENCING is a state-of-the-art genetic testing method that allows for the detection of mutations in the RB1 gene with a high degree of accuracy. This test is recommended for individuals with a family history of retinoblastoma or those who have been diagnosed with the condition.

The cost of the Nx GEN SEQUENCING test for hereditary retinoblastoma in India is INR 28,665.

Why Choose DNA Labs India for Hereditary Retinoblastoma Testing?

At DNA Labs India, we are committed to providing accurate and reliable genetic testing services for a wide range of conditions, including hereditary retinoblastoma. Our team of experienced geneticists uses state-of-the-art technology and techniques to ensure the highest level of accuracy and precision in our testing processes.

In addition, we offer competitive pricing and fast turnaround times for all of our genetic testing services, making it easy and affordable to get the answers you need to make informed decisions about your health.

Conclusion

If you or a loved one has been diagnosed with retinoblastoma or has a family history of the condition, genetic testing may be recommended to identify any potential mutations in the RB1 gene. The Nx GEN SEQUENCING test is a highly accurate and reliable method for detecting these mutations, and DNA Labs India is proud to offer this service at an affordable price.

Contact us today to learn more about our genetic testing services and how we can help you get the answers you need.

Retinoblastoma is a rare type of eye cancer that usually develops in retina during early childhood typically before the age of 5 years. Hereditary Retinoblastoma is mainly caused by a mutation in a RB1 gene that controls cell division. This test is useful for the genetic determination of this disorder.