Short Description

NGS genetic DNA test detecets for variant and mutation detection in NBN gene for Nijmegen breakage syndrome

PreTest Information

Clinical History of Patient who is going for NBN Gene Nijmegen breakage syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NBN Gene Nijmegen breakage syndrome NGS Genetic DNA Test gene NBN

Detail Description

NBN Gene Nijmegen Breakage Syndrome NGS Genetic DNA Test

NBN Gene Nijmegen Breakage Syndrome (NBS) is a rare genetic disorder that affects the body's ability to repair damaged DNA. This condition is caused by mutations in the NBN gene, which provides instructions for making a protein called nibrin that is involved in repairing DNA damage.

The NBS can cause a wide range of symptoms, including growth delays, intellectual disability, increased cancer risk, and immune system dysfunction. The symptoms of NBS can vary widely depending on the severity of the mutations in the NBN gene.

Symptoms of NBN Gene Nijmegen Breakage Syndrome

The symptoms of NBN Gene Nijmegen Breakage Syndrome can vary from person to person. Some common symptoms of the condition include:

• Delayed growth and development
• Small head size
• Intellectual disability
• Increased risk of cancer, including leukemia and lymphoma
• Immune system dysfunction
• Sensitivity to radiation

Diagnosis of NBN Gene Nijmegen Breakage Syndrome

The diagnosis of NBN Gene Nijmegen Breakage Syndrome is usually made based on the symptoms that a person is experiencing, as well as their family history. Genetic testing can also be used to confirm a diagnosis of NBS.

The NGS Genetic DNA Test is a genetic test that can be used to identify mutations in the NBN gene. This test involves taking a small sample of blood or saliva and analyzing the DNA for mutations in the NBN gene. The NGS Genetic DNA Test is a highly accurate and reliable test that can provide a definitive diagnosis of NBN Gene Nijmegen Breakage Syndrome.

Cost of NGS Genetic DNA Test for NBN Gene Nijmegen Breakage Syndrome

The cost of the NGS Genetic DNA Test for NBN Gene Nijmegen Breakage Syndrome is INR 20,000. This test is not covered by most insurance plans, so patients will need to pay for the test out of pocket.

While the cost of the NGS Genetic DNA Test may seem expensive, it is important to keep in mind that early diagnosis of NBN Gene Nijmegen Breakage Syndrome can lead to better outcomes for patients. By identifying the condition early, doctors can develop a treatment plan that can help manage symptoms and reduce the risk of complications.

Conclusion

NBN Gene Nijmegen Breakage Syndrome is a rare genetic disorder that can cause a wide range of symptoms, including growth delays, intellectual disability, increased cancer risk, and immune system dysfunction. The NGS Genetic DNA Test is a highly accurate and reliable test that can be used to diagnose NBN Gene Nijmegen Breakage Syndrome. While the cost of the test may seem expensive, early diagnosis can lead to better outcomes for patients. If you suspect that you or a loved one may have NBN Gene Nijmegen Breakage Syndrome, it is important to talk to your doctor about the NGS Genetic DNA Test and other diagnostic options.

At DNA Labs India, we provide comprehensive genetic testing services, including the NGS Genetic DNA Test for NBN Gene Nijmegen Breakage Syndrome. Our team of experienced genetic counselors and technicians can help you understand your test results and develop a treatment plan that is tailored to your unique needs. Contact us today to schedule your NGS Genetic DNA Test.