Short Description

NGS genetic DNA test detecets for variant and mutation detection in WRN gene for Werner syndrome

PreTest Information

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

Detail Description

Understanding Werner Syndrome: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Werner syndrome is a rare genetic disorder that causes premature aging in individuals. The disease is caused by a mutation in the WRN gene, which is responsible for repairing damaged DNA. Werner syndrome is most commonly diagnosed in people of European or Japanese descent, and symptoms usually appear in the late teenage years or early 20s.

Symptoms of Werner Syndrome

The symptoms of Werner syndrome can vary from person to person, but typically include:

• Gray hair and hair loss
• Wrinkled skin and thinning skin
• Loss of muscle mass and strength
• Joint stiffness and pain
• Cataracts and other vision problems
• Diabetes and other metabolic disorders

Individuals with Werner syndrome also have an increased risk of developing certain types of cancer, including sarcomas and thyroid cancer.

Diagnosis of Werner Syndrome

Diagnosis of Werner syndrome is typically based on clinical symptoms and family history. A genetic test can also be used to confirm the presence of a WRN gene mutation. This test involves analyzing a blood or saliva sample for changes in the DNA sequence of the WRN gene.

NGS Genetic DNA Test Cost in India

The cost of an NGS genetic DNA test for Werner syndrome in India is approximately INR 20,000. This test uses next-generation sequencing (NGS) technology to analyze the entire coding region of the WRN gene, allowing for a more comprehensive analysis of potential mutations.

NGS technology is a powerful tool for genetic testing, as it allows for the simultaneous analysis of multiple genes and can detect even low-frequency mutations. This makes it an ideal tool for diagnosing rare genetic disorders like Werner syndrome.

Conclusion

Werner syndrome is a rare genetic disorder that causes premature aging and an increased risk of certain types of cancer. Diagnosis is typically based on clinical symptoms and confirmed with a genetic test. The cost of an NGS genetic DNA test for Werner syndrome in India is approximately INR 20,000. With the power of NGS technology, individuals can receive a more comprehensive analysis of potential mutations and a more accurate diagnosis of this rare disorder.

If you suspect that you or a loved one may have Werner syndrome, it is important to speak with a genetic counselor or healthcare provider to discuss testing options and potential treatment options.

At DNA Labs India, we provide a variety of genetic testing services, including NGS genetic DNA testing for rare disorders like Werner syndrome. Our team of expert genetic counselors and laboratory technicians are committed to providing accurate and reliable results to help individuals and families make informed decisions about their health. Contact us today to learn more about our services.

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 WRN Gene Werner syndrome NGS Genetic DNA Test