Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGA gene for Afibrinogenemia, congenital

PreTest Information

Clinical History of Patient who is going for FGA Gene Afibrinogenemia, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGA Gene Afibrinogenemia, congenital NGS Genetic DNA Test gene FGA

Detail Description

FGA Gene Afibrinogenemia: Symptoms, Diagnosis and NGS Genetic DNA Test Cost in India

FGA gene afibrinogenemia is a rare congenital disorder that affects the ability of blood to clot. This condition is caused by mutations in the FGA gene, which provides instructions for making a protein called fibrinogen. Fibrinogen is an essential component of blood clotting, and its absence or deficiency can cause bleeding episodes.

Symptoms of FGA Gene Afibrinogenemia

The symptoms of FGA gene afibrinogenemia can vary depending on the severity of the condition. Some individuals may have no symptoms at all, while others may experience excessive bleeding or bruising. The most common symptoms include:

• Nosebleeds
• Heavy menstrual bleeding
• Bleeding gums
• Easy bruising
• Blood in the urine or stool

Diagnosis of FGA Gene Afibrinogenemia

Diagnosis of FGA gene afibrinogenemia is typically done through a blood test that measures the level of fibrinogen in the blood. If the fibrinogen level is low or absent, genetic testing may be performed to identify the specific mutation in the FGA gene that is causing the condition.

NGS Genetic DNA Test Cost in India

NGS genetic DNA testing is a powerful tool for identifying genetic mutations that cause rare diseases like FGA gene afibrinogenemia. The cost of NGS genetic DNA testing in India can vary depending on the specific test being performed and the laboratory conducting the test. However, the average cost of NGS genetic DNA testing for FGA gene afibrinogenemia in India is around INR 20,000.

It is important to note that NGS genetic DNA testing is not always covered by insurance, and patients may need to pay out of pocket for the test.

Conclusion

FGA gene afibrinogenemia is a rare congenital disorder that can cause bleeding episodes. Diagnosis of the condition is typically done through a blood test that measures the level of fibrinogen in the blood, and genetic testing may be performed to identify the specific mutation in the FGA gene that is causing the condition. NGS genetic DNA testing is a powerful tool for identifying genetic mutations and can be useful in diagnosing rare diseases like FGA gene afibrinogenemia. The cost of NGS genetic DNA testing in India for FGA gene afibrinogenemia is around INR 20,000, but patients should be aware that the cost may vary depending on the specific test being performed and the laboratory conducting the test.

If you suspect that you or a loved one may have FGA gene afibrinogenemia, it is important to speak with a healthcare provider as soon as possible to discuss testing and treatment options.