Short Description

NGS genetic DNA test detecets for variant and mutation detection in VHL gene for von Hippel-Lindau syndrome

PreTest Information

Clinical History of Patient who is going for VHL Gene von Hippel-Lindau syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with VHL Gene von Hippel-Lindau syndrome NGS Genetic DNA Test gene VHL

Detail Description

VHL Gene von Hippel-Lindau syndrome NGS Genetic DNA Test cost INR:20000 symptoms diagnosis

Von Hippel-Lindau (VHL) syndrome is a rare genetic disorder that affects approximately 1 in 36,000 people worldwide. It is caused by a mutation in the VHL gene, which is responsible for producing a protein that helps regulate cell growth and division. Individuals with VHL syndrome are at an increased risk for developing tumors and cysts in various parts of the body, including the brain, spine, kidneys, and adrenal glands.

Symptoms of VHL syndrome

The symptoms of VHL syndrome can vary depending on the location and size of the tumors or cysts. Some of the most common symptoms include:

• Headaches
• Dizziness
• Hearing loss
• Blurred vision
• Abdominal pain
• Blood in the urine
• High blood pressure
• Weakness or numbness in the limbs

Diagnosis of VHL syndrome

Diagnosing VHL syndrome can be challenging because the symptoms can be vague and nonspecific. A diagnosis is typically made based on a combination of the patient's medical history, physical examination, and imaging tests such as CT scans and MRIs. Genetic testing can also be used to confirm a diagnosis of VHL syndrome.

NGS Genetic DNA Test for VHL syndrome

The NGS Genetic DNA Test is a powerful tool for diagnosing VHL syndrome. This test uses next-generation sequencing technology to analyze the patient's DNA and identify any mutations in the VHL gene. The test is highly accurate and can detect even small mutations that may be missed by other testing methods.

Cost of NGS Genetic DNA Test for VHL syndrome

The cost of the NGS Genetic DNA Test for VHL syndrome is approximately INR 20,000. This cost may vary depending on the laboratory and location where the test is performed. It is important to check with your insurance provider to see if the test is covered under your plan.

Conclusion

VHL syndrome is a rare genetic disorder that can have serious health consequences if left untreated. Early diagnosis and treatment are essential for improving outcomes and reducing the risk of complications. The NGS Genetic DNA Test is a valuable tool for diagnosing VHL syndrome and should be considered for individuals who are at risk for this condition.

At DNA Labs India, we offer a wide range of genetic testing services, including the NGS Genetic DNA Test for VHL syndrome. Contact us today to learn more about our testing options and how we can help you manage your health.