Short Description

NGS genetic DNA test detecets for variant and mutation detection in LRP5 gene for Osteoporosis pseudoglioma syndrome

PreTest Information

Clinical History of Patient who is going for LRP5 Gene Osteoporosis pseudoglioma syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LRP5 Gene Osteoporosis pseudoglioma syndrome NGS Genetic DNA Test gene LRP5

Detail Description

LRP5 Gene and Osteoporosis Pseudoglioma Syndrome: NGS Genetic DNA Test Cost and Diagnosis in India

Osteoporosis Pseudoglioma Syndrome (OPPG) is a rare genetic disorder that affects bone and eye development. The syndrome is caused by mutations in the LRP5 gene, which plays a crucial role in bone density regulation. Individuals with OPPG have low bone density and are prone to fractures. They also have eye abnormalities, such as blindness or severe vision impairment.

If you suspect that you or a loved one may have OPPG, getting tested for LRP5 gene mutations is crucial. In this blog, we'll discuss the symptoms, diagnosis, and cost of NGS genetic DNA testing for LRP5 gene mutations in India.

Symptoms of OPPG

OPPG is a rare disorder and can be difficult to diagnose. However, there are some common symptoms that may indicate the presence of the syndrome. These include:

• Low bone density
• Frequent fractures, especially in childhood
• Eye abnormalities, such as blindness or severe vision impairment
• Short stature
• Intellectual disability (in some cases)

If you or a loved one is experiencing any of these symptoms, it is important to consult a healthcare professional for further evaluation.

Diagnosis of OPPG

Diagnosing OPPG can be challenging, as the symptoms are similar to other bone and eye disorders. However, genetic testing can confirm the presence of LRP5 gene mutations. Next-generation sequencing (NGS) is a highly accurate and efficient way to detect genetic mutations, including LRP5 gene mutations.

The NGS genetic DNA test for LRP5 gene mutations involves collecting a blood or saliva sample from the patient and analyzing it in a laboratory. The test can detect mutations in the LRP5 gene with high accuracy, allowing for an accurate diagnosis of OPPG.

Cost of NGS Genetic DNA Testing for LRP5 Gene Mutations in India

The cost of NGS genetic DNA testing for LRP5 gene mutations in India varies depending on the testing facility and the specific test being performed. On average, the cost of the test is around INR 20,000.

It is important to note that genetic testing may not be covered by insurance, so it is important to check with your provider before getting tested.

Conclusion

OPPG is a rare genetic disorder that can have serious consequences for bone and eye health. If you or a loved one is experiencing symptoms of OPPG, getting tested for LRP5 gene mutations is crucial for an accurate diagnosis. NGS genetic DNA testing is a highly accurate and efficient way to detect LRP5 gene mutations, and the cost of the test in India is around INR 20,000. If you suspect that you or a loved one may have OPPG, consult a healthcare professional for further evaluation and testing.

At DNA Labs India, we offer highly accurate and reliable NGS genetic DNA testing for LRP5 gene mutations. Contact us today to learn more about our testing services and how we can help you get the answers you need.

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 LRP5 Gene Osteoporosis pseudoglioma syndrome NGS Genetic DNA Test