Short Description

NGS genetic DNA test detecets for variant and mutation detection in FOXC1 gene for Axenfeld-Rieger syndrome type 3

PreTest Information

Clinical History of Patient who is going for FOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic DNA Test gene FOXC1

Detail Description

FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test

FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 is a rare genetic disorder that affects the eyes, teeth, and facial development. It is caused by mutations in the FOXC1 gene, which provides instructions for making a protein that is essential for the normal development of these tissues. Symptoms of Axenfeld-Rieger Syndrome Type 3 include:

• Eye abnormalities such as glaucoma, cataracts, and iris abnormalities
• Dental abnormalities such as missing or extra teeth
• Facial abnormalities such as a flattened mid-face and a small lower jaw

Diagnosis of Axenfeld-Rieger Syndrome Type 3 is usually based on the presence of these symptoms, as well as genetic testing to confirm the presence of a FOXC1 gene mutation. The NGS Genetic DNA Test is a highly accurate and reliable method of detecting these mutations.

Cost of the FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test

The cost of the FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test is INR 20,000. This includes the cost of the test itself, as well as any necessary genetic counseling and interpretation of the results.

Benefits of the FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test

The FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test provides several benefits for individuals and families affected by this condition, including:

• Accurate and reliable diagnosis of Axenfeld-Rieger Syndrome Type 3
• Identification of family members who may be at risk of developing the condition
• Early detection and intervention for eye and dental abnormalities
• Improved understanding of the condition and its potential complications

Conclusion

If you or a family member are experiencing symptoms of Axenfeld-Rieger Syndrome Type 3, genetic testing may be a valuable tool for diagnosis and management of this condition. The FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test is a highly accurate and reliable method of detecting mutations in the FOXC1 gene, and can provide important information for individuals and families affected by this rare genetic disorder.

Contact DNA Labs India today to learn more about the FOXC1 Gene Axenfeld-Rieger Syndrome Type 3 NGS Genetic DNA Test and how it can benefit you and your family.