Short Description

NGS genetic DNA test detecets for variant and mutation detection in CFC1 gene for Heterotaxy, visceral type 2

PreTest Information

Clinical History of Patient who is going for CFC1 Gene Heterotaxy, visceral type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFC1 Gene Heterotaxy, visceral type 2 NGS Genetic DNA Test gene CFC1

Detail Description

CFC1 Gene Heterotaxy, Visceral Type 2 NGS Genetic DNA Test

CFC1 gene heterotaxy, visceral type 2 is a rare genetic condition that affects the development of organs in the body. It is caused by mutations in the CFC1 gene and can lead to a variety of symptoms and health problems. If you suspect that you or a loved one may have this condition, it is important to seek out testing and diagnosis to ensure proper treatment and care.

Symptoms of CFC1 Gene Heterotaxy, Visceral Type 2

The symptoms of CFC1 gene heterotaxy, visceral type 2 can vary greatly from person to person. Some common symptoms include:

• Abnormal placement of organs in the body
• Heart defects
• Liver problems
• Digestive issues
• Respiratory problems
• Delayed growth and development

If you or a loved one are experiencing any of these symptoms, it is important to seek out testing and diagnosis to determine if CFC1 gene heterotaxy, visceral type 2 is the underlying cause.

Diagnosis of CFC1 Gene Heterotaxy, Visceral Type 2

Diagnosing CFC1 gene heterotaxy, visceral type 2 typically involves a combination of physical exams, imaging tests, and genetic testing. Your doctor may perform an ultrasound, MRI, or CT scan to assess the placement and function of your organs. They may also perform genetic testing to check for mutations in the CFC1 gene.

NGS Genetic DNA Test

NGS genetic DNA testing is a powerful tool for diagnosing genetic conditions like CFC1 gene heterotaxy, visceral type 2. NGS stands for next-generation sequencing, which refers to a type of DNA sequencing technology that allows for faster and more accurate analysis of genetic information. This type of testing can help identify mutations in the CFC1 gene that may be causing symptoms.

Cost of NGS Genetic DNA Test

The cost of an NGS genetic DNA test for CFC1 gene heterotaxy, visceral type 2 can vary depending on the provider and location. At DNA Labs India, we offer this test for INR 20,000. We understand that genetic testing can be a significant expense, which is why we strive to keep our prices as affordable as possible without compromising on quality or accuracy.

Conclusion

CFC1 gene heterotaxy, visceral type 2 is a rare genetic condition that can lead to a variety of symptoms and health problems. If you or a loved one are experiencing any of the symptoms associated with this condition, it is important to seek out testing and diagnosis to ensure proper treatment and care. NGS genetic DNA testing can be a powerful tool for diagnosing this condition, and at DNA Labs India, we offer this test for INR 20,000.

Remember, early detection and treatment can make a big difference in managing symptoms and improving quality of life for those with CFC1 gene heterotaxy, visceral type 2.

CFC1 (Cripto, FRL-1, Cryptic Family 1) is a gene that encodes a protein involved in the Nodal signaling pathway, which plays a critical role in embryonic development and left-right axis determination. Mutations in the CFC1 gene can disrupt the Nodal signaling pathway and contribute to the development of Heterotaxy, Visceral Type 2.

NGS (Next-Generation Sequencing) genetic DNA tests can be used to analyze the DNA sequence of genes like CFC1 to identify any mutations or variants that may be associated with Heterotaxy, Visceral Type 2.

If you or someone you know is considering genetic testing for Heterotaxy, Visceral Type 2 related to the CFC1 gene, I recommend consulting with a medical geneticist, a pediatrician, or a genetic counselor. They can provide accurate and current information about the condition, the implications of genetic testing, and any available treatment or management options. Medical knowledge can evolve, so it's important to rely on expert guidance for the latest information.