Short Description

NGS genetic DNA test detecets for variant and mutation detection in MSX2 gene for Craniosynostosis type 2

PreTest Information

Clinical History of Patient who is going for MSX2 Gene Craniosynostosis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSX2 Gene Craniosynostosis type 2 NGS Genetic DNA Test gene MSX2

Detail Description

MSX2 Gene Craniosynostosis Type 2 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

MSX2 gene craniosynostosis type 2 is a genetic disorder that affects the development of the skull and brain. It is a rare condition that occurs in approximately 1 in 10,000 births. The MSX2 gene provides instructions for making a protein that is involved in the development of bones in the skull and face. When this gene is mutated, it can cause premature fusion of the skull bones, leading to craniosynostosis.

Symptoms of MSX2 Gene Craniosynostosis Type 2

The symptoms of MSX2 gene craniosynostosis type 2 can vary from mild to severe. The most common symptoms include:

• Abnormal head shape
• Increased pressure inside the skull
• Delayed development of motor skills
• Speech and language delays
• Learning difficulties

Diagnosis of MSX2 Gene Craniosynostosis Type 2

Diagnosis of MSX2 gene craniosynostosis type 2 is usually made through physical examination and imaging tests such as CT scans or MRI. Genetic testing can also be used to confirm the diagnosis and identify the specific mutation in the MSX2 gene.

NGS Genetic DNA Test for MSX2 Gene Craniosynostosis Type 2

NGS genetic DNA testing is a powerful tool for identifying genetic mutations associated with MSX2 gene craniosynostosis type 2. This test uses next-generation sequencing technology to analyze the DNA sequence of the MSX2 gene and identify any mutations that may be present.

Cost of MSX2 Gene Craniosynostosis Type 2 NGS Genetic DNA Test

The cost of MSX2 gene craniosynostosis type 2 NGS genetic DNA test in India is INR 20,000. This cost may vary depending on the laboratory and location.

Conclusion

MSX2 gene craniosynostosis type 2 is a rare genetic disorder that can cause premature fusion of the skull bones. Symptoms can vary from mild to severe, and diagnosis is usually made through physical examination and imaging tests. NGS genetic DNA testing is a powerful tool for identifying genetic mutations associated with MSX2 gene craniosynostosis type 2, and the cost of this test in India is INR 20,000.

If you suspect that you or a loved one may have MSX2 gene craniosynostosis type 2, it is important to speak with a healthcare professional for diagnosis and treatment options.

For more information on genetic testing and DNA labs in India, please visit DNA Labs India.