Short Description

NGS genetic DNA test detecets for variant and mutation detection in MSX2 gene for Parietal foramina type 1

PreTest Information

Clinical History of Patient who is going for MSX2 Gene Parietal foramina type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSX2 Gene Parietal foramina type 1 NGS Genetic DNA Test gene MSX2

Detail Description

MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test: Symptoms, Diagnosis and Cost in India

MSX2 gene parietal foramina type 1 is a rare genetic disorder that affects the development of the skull bones. This disorder is caused by mutations in the MSX2 gene, which provides instructions for making a protein that is essential for bone formation and development. Individuals with this disorder typically have small holes, or foramina, in the parietal bones of their skull. These foramina are not harmful and do not cause any symptoms, but they can be detected through imaging tests such as X-rays or CT scans.

Symptoms of MSX2 Gene Parietal Foramina Type 1

As mentioned earlier, individuals with this disorder typically do not have any symptoms other than the presence of small holes in their skull bones. However, in rare cases, some individuals may experience mild skull abnormalities or cranial nerve dysfunction.

Diagnosis of MSX2 Gene Parietal Foramina Type 1

Diagnosis of this disorder is usually made through imaging tests such as X-rays or CT scans that reveal the presence of small holes in the parietal bones. Genetic testing can also be done to confirm the diagnosis by identifying mutations in the MSX2 gene.

NGS Genetic DNA Test for MSX2 Gene Parietal Foramina Type 1

Next-generation sequencing (NGS) genetic DNA testing is a highly accurate and efficient method of identifying mutations in the MSX2 gene that cause parietal foramina type 1. This test involves sequencing the entire MSX2 gene to detect any mutations or changes in the DNA sequence. NGS testing is a non-invasive and painless procedure that involves collecting a small sample of blood or saliva from the patient. The results of the test can confirm the diagnosis of parietal foramina type 1 and provide information about the specific mutations present in the MSX2 gene.

Cost of MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test in India

The cost of NGS genetic DNA testing for MSX2 gene parietal foramina type 1 in India can vary depending on the laboratory and location. On average, the cost of this test in India is around INR 20,000. It is important to note that this cost may not include additional fees for consultation with a genetic counselor or other healthcare professional.

Conclusion

MSX2 gene parietal foramina type 1 is a rare genetic disorder that can be diagnosed through imaging tests or genetic testing. NGS genetic DNA testing is a highly accurate and efficient method of identifying mutations in the MSX2 gene that cause this disorder. The cost of this test in India is around INR 20,000. If you suspect that you or a loved one may have this disorder, it is important to consult with a healthcare professional for proper diagnosis and management.

At DNA Labs India, we offer NGS genetic DNA testing for MSX2 gene parietal foramina type 1 and other genetic disorders. Our state-of-the-art laboratory and experienced team of geneticists ensure accurate and reliable results for our clients. Contact us today to learn more about our services and how we can help you.

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 MSX2 Gene Parietal foramina type 1 NGS Genetic DNA Test