Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGFR2 gene for Saethre-Chotzen syndrome

PreTest Information

Clinical History of Patient who is going for FGFR2 Gene Saethre-Chotzen syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Saethre-Chotzen syndrome NGS Genetic DNA Test gene FGFR2

Detail Description

FGFR2 Gene and Saethre-Chotzen Syndrome: NGS Genetic DNA Test Cost INR 20,000

Saethre-Chotzen Syndrome is a genetic disorder that affects the development of bones in the skull and face. It is caused by mutations in the FGFR2 gene, which provides instructions for making a protein that is involved in the growth and development of bone and other tissues.

Individuals with Saethre-Chotzen Syndrome may have a variety of symptoms, including:

• Abnormal shape of the skull
• Facial abnormalities
• Abnormalities of the hands and feet
• Vision and hearing problems

Diagnosis of Saethre-Chotzen Syndrome is typically made based on physical examination and genetic testing. Next-generation sequencing (NGS) is a powerful tool for genetic testing, as it allows for the rapid and accurate analysis of large amounts of DNA sequence data.

DNA Labs India offers an NGS genetic DNA test for the FGFR2 gene, which can be used to diagnose Saethre-Chotzen Syndrome. The cost of this test is INR 20,000.

If you or a loved one is experiencing symptoms of Saethre-Chotzen Syndrome, it is important to seek medical attention and undergo genetic testing to receive an accurate diagnosis. Early diagnosis and treatment can help to manage symptoms and improve quality of life.

In addition to genetic testing, individuals with Saethre-Chotzen Syndrome may benefit from a multidisciplinary approach to treatment, which may include surgery, physical therapy, and other supportive measures.

Contact DNA Labs India to learn more about our NGS genetic DNA test for the FGFR2 gene and to schedule your test today.