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FGA Gene Afibrinogenemia congenital Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The FGA Gene Afibrinogenemia Congenital Genetic Test is a specialized diagnostic procedure designed to identify mutations in the FGA gene, which are responsible for congenital afibrinogenemia. This rare genetic disorder is characterized by the absence or extremely low levels of fibrinogen, a crucial protein in the blood clotting process. Individuals with congenital afibrinogenemia are at risk of excessive bleeding from minor injuries, spontaneous bleeding, and other serious bleeding complications.

Performed at DNA Labs UAE, this test involves analyzing the patient’s DNA to detect specific mutations in the FGA gene that cause the disorder. The process is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management strategies for affected individuals. The test is also valuable for family planning and genetic counseling for families with a history of the condition.

The cost of the FGA Gene Afibrinogenemia Congenital Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the FGA gene. Patients and healthcare providers considering this test are encouraged to consult with DNA Labs UAE for the most current information and to discuss how this test fits into the overall management plan for congenital afibrinogenemia.

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FGA Gene Afibrinogenemia Congenital Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory specializing in genetic testing. Today, we will be discussing the FGA Gene Afibrinogenemia Congenital Genetic Test, including its cost, symptoms, diagnosis, and other important details.

Test Name: FGA Gene Afibrinogenemia Congenital Genetic Test

Components:

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Hematology
  • Doctor: Hematologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the FGA Gene Afibrinogenemia Congenital Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the FGA Gene Afibrinogenemia Congenital Genetic Test gene FGA.

Test Details

FGA gene afibrinogenemia is a rare genetic disorder characterized by the absence or deficiency of fibrinogen, a blood clotting protein. This condition is caused by mutations in the FGA gene, which provides instructions for making one of the three subunits of fibrinogen.

Congenital NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of FGA gene afibrinogenemia, this test can identify mutations or variants in the FGA gene and other relevant genes associated with afibrinogenemia.

The NGS genetic test for FGA gene afibrinogenemia involves obtaining a DNA sample, usually through a blood sample, from the affected individual. The DNA is then sequenced to identify any genetic changes or mutations that may be responsible for the disorder.

The test results can help in confirming the diagnosis of afibrinogenemia and determining the specific genetic mutation present in the FGA gene. This information is important for genetic counseling, understanding the inheritance pattern, and guiding appropriate management and treatment options for individuals with afibrinogenemia.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. If you suspect that you or a family member may have FGA gene afibrinogenemia, we encourage you to consult with a hematologist and consider undergoing the FGA Gene Afibrinogenemia Congenital Genetic Test.

Test Name FGA Gene Afibrinogenemia congenital Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test 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
Test Details

FGA gene afibrinogenemia is a rare genetic disorder characterized by the absence or deficiency of fibrinogen, a blood clotting protein. It is caused by mutations in the FGA gene, which provides instructions for making one of the three subunits of fibrinogen.

Congenital NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. This test can identify mutations or variants in the FGA gene and other relevant genes associated with afibrinogenemia.

The NGS genetic test for FGA gene afibrinogenemia involves obtaining a DNA sample, usually through a blood sample, from the affected individual. The DNA is then sequenced to identify any genetic changes or mutations that may be responsible for the disorder.

The test results can help in confirming the diagnosis of afibrinogenemia and determining the specific genetic mutation present in the FGA gene. This information is important for genetic counseling, understanding the inheritance pattern, and guiding appropriate management and treatment options for individuals with afibrinogenemia.

SKU: TEST-3850 Category:

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