Short Description

NGS genetic DNA test detecets for variant and mutation detection in FAM20C gene for Raine syndrome

PreTest Information

Clinical History of Patient who is going for FAM20C Gene Raine syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FAM20C Gene Raine syndrome NGS Genetic DNA Test gene FAM20C

Detail Description

FAM20C Gene Raine Syndrome NGS Genetic DNA Test Cost - DNA Labs India

Raine Syndrome is a rare genetic disorder that affects bone development and growth. It is caused by mutations in the FAM20C gene, which plays an important role in the mineralization of bones and teeth. The condition is characterized by a number of physical abnormalities, including a small head, short stature, and malformed bones.

At DNA Labs India, we offer an NGS Genetic DNA Test that can help diagnose Raine Syndrome by analyzing the FAM20C gene. The test is quick and easy, requiring only a small blood or saliva sample from the patient. Results are typically available within a few weeks.

Cost of the NGS Genetic DNA Test for Raine Syndrome

The cost of our NGS Genetic DNA Test for Raine Syndrome is INR 20,000. This includes the cost of the test itself, as well as any necessary consultations with our team of genetic counselors and physicians.

Symptoms of Raine Syndrome

The symptoms of Raine Syndrome can vary widely from person to person, but some of the most common include:

• Small head size
• Short stature
• Abnormal bone growth and development
• Malformed bones, particularly in the hands and feet
• Widely spaced eyes
• Low-set ears

If you or a loved one are experiencing any of these symptoms, it may be worth considering genetic testing to determine if Raine Syndrome is the cause.

Diagnosing Raine Syndrome

Diagnosing Raine Syndrome can be challenging, as it is a rare disorder and the symptoms can be similar to those of other conditions. Genetic testing is often the most effective way to determine if a patient has Raine Syndrome, as it can identify mutations in the FAM20C gene that are associated with the condition.

At DNA Labs India, we are committed to providing accurate and reliable genetic testing services to help patients and their families get the answers they need. If you are concerned about Raine Syndrome or any other genetic disorder, please don't hesitate to contact us to learn more about our testing options.

Raine syndrome is a very rare genetic disorder characterized by a range of physical and developmental abnormalities. Mutations in the FAM20C gene are associated with this condition.

The FAM20C gene provides instructions for producing a protein that is involved in various cellular processes, including the formation of bone and teeth. Mutations in this gene can disrupt normal bone and teeth development, leading to the features associated with Raine syndrome.

An NGS (Next-Generation Sequencing) genetic DNA test for the FAM20C gene involves sequencing the DNA to identify any mutations or variations within the gene that could be linked to Raine syndrome. This testing can help diagnose the condition and identify individuals who carry mutations in the FAM20C gene.

If you suspect that you or someone you know may have Raine syndrome or if there's a family history of the condition, it's important to consult with a healthcare professional, such as a geneticist or a pediatrician. They can guide you through the genetic testing process, interpret the results, and provide appropriate recommendations for management and treatment based on the specific genetic findings.