Short Description

NGS genetic DNA test detecets for variant and mutation detection in TBX15 gene for Cousin syndrome

PreTest Information

Clinical History of Patient who is going for TBX15 Gene Cousin syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX15 Gene Cousin syndrome NGS Genetic DNA Test gene TBX15

Detail Description

TBX15 Gene Cousin Syndrome NGS Genetic DNA Test: Symptoms, Diagnosis, and Cost

Are you or your loved one experiencing symptoms of Cousin syndrome? TBX15 gene Cousin syndrome is a rare genetic disorder that affects the development of bones and joints. It is caused by a mutation in the TBX15 gene. If left untreated, it can lead to severe physical disabilities and chronic pain. Early diagnosis is crucial for effective treatment. This is where NGS genetic DNA testing comes in.

What is NGS Genetic DNA Testing?

NGS genetic DNA testing is a sophisticated diagnostic test that analyzes the DNA sequence of an individual. It is a powerful tool for identifying genetic disorders that traditional testing methods may not detect. NGS testing can detect mutations in genes that are associated with various genetic disorders, including Cousin syndrome.

What are the Symptoms of Cousin Syndrome?

The symptoms of Cousin syndrome vary from person to person. However, some common symptoms include:

• Short stature
• Abnormal curvature of the spine (scoliosis)
• Abnormal curvature of the fingers (clinodactyly)
• Abnormal curvature of the toes (brachydactyly)
• Joint pain and stiffness
• Difficulty walking

If you or your loved one is experiencing any of these symptoms, it is essential to consult a doctor for proper diagnosis and treatment.

Diagnosis of Cousin Syndrome

The diagnosis of Cousin syndrome involves a thorough physical examination, medical history, and genetic testing. NGS genetic DNA testing is the most accurate and reliable method for diagnosing Cousin syndrome. It can detect mutations in the TBX15 gene, which is associated with Cousin syndrome.

Cost of NGS Genetic DNA Test for Cousin Syndrome

The cost of NGS genetic DNA testing for Cousin syndrome in India varies depending on the laboratory and location. However, on average, the cost of NGS genetic DNA testing for Cousin syndrome is around INR 20,000.

Conclusion

Cousin syndrome is a rare genetic disorder that can cause severe physical disabilities and chronic pain. Early diagnosis is crucial for effective treatment. NGS genetic DNA testing is a powerful tool for identifying genetic disorders, including Cousin syndrome. If you or your loved one is experiencing symptoms of Cousin syndrome, consult a doctor for proper diagnosis and treatment.

At DNA Labs India, we offer NGS genetic DNA testing for Cousin syndrome and other genetic disorders. Our state-of-the-art laboratory and experienced team of geneticists ensure accurate and reliable results. Contact us today to schedule an appointment.