Short Description

NGS genetic DNA test detecets for variant and mutation detection in FLNB gene for Spondylocarpotarsal synostosis syndrome

PreTest Information

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

Detail Description

FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic DNA Test

FLNB Gene Spondylocarpotarsal synostosis syndrome is a rare genetic disorder that affects skeletal development. It is caused by mutations in the FLNB gene. The FLNB gene provides instructions for making a protein called filamin B, which is important for the development and maintenance of bones and other tissues in the body.

Individuals with FLNB Gene Spondylocarpotarsal synostosis syndrome have fused vertebrae in the neck and spine, which can cause stiffness and limited movement. They may also have fused bones in the hands and feet, which can cause difficulty with movement and dexterity. Other symptoms may include scoliosis, hip dysplasia, and hearing loss.

The diagnosis of FLNB Gene Spondylocarpotarsal synostosis syndrome is usually made based on clinical features and confirmed by genetic testing. Next-generation sequencing (NGS) genetic DNA testing is a powerful tool for identifying mutations in the FLNB gene.

Cost of FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic DNA Test

The cost of FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic DNA Test in India is INR 20,000. This test is available at DNA Labs India, a leading provider of genetic testing services in the country.

Symptoms of FLNB Gene Spondylocarpotarsal synostosis syndrome

The symptoms of FLNB Gene Spondylocarpotarsal synostosis syndrome may vary from person to person, but typically include:

• Fused vertebrae in the neck and spine
• Fused bones in the hands and feet
• Scoliosis
• Hip dysplasia
• Hearing loss

Individuals with FLNB Gene Spondylocarpotarsal synostosis syndrome may also experience stiffness, limited movement, and difficulty with dexterity.

Diagnosis of FLNB Gene Spondylocarpotarsal synostosis syndrome

The diagnosis of FLNB Gene Spondylocarpotarsal synostosis syndrome is typically made based on clinical features, such as fused bones in the hands and feet, and confirmed by genetic testing. Next-generation sequencing (NGS) genetic DNA testing is a powerful tool for identifying mutations in the FLNB gene.

If you or a loved one are experiencing symptoms of FLNB Gene Spondylocarpotarsal synostosis syndrome, it is important to speak with a healthcare professional. DNA Labs India offers FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic DNA Test at an affordable cost of INR 20,000. Early diagnosis can help individuals with FLNB Gene Spondylocarpotarsal synostosis syndrome receive appropriate care and support.

At DNA Labs India, we are committed to providing our clients with accurate, reliable, and affordable genetic testing services. Contact us today to learn more about our FLNB Gene Spondylocarpotarsal synostosis syndrome NGS Genetic DNA Test and other genetic testing services.