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FANCG Gene Fanconi anemia type G Genetic Test

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

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The FANCG Gene Fanconi Anemia Type G Genetic Test is a specialized diagnostic procedure designed to identify mutations in the FANCG gene, which are implicated in the development of Fanconi anemia type G, a rare genetic disorder. This condition is part of a group of inherited diseases that affect the bone marrow, leading to decreased production of all types of blood cells. Fanconi anemia type G is characterized by physical abnormalities, bone marrow failure, and increased risk for certain types of cancer.

The test involves analyzing the patient’s DNA to look for specific mutations in the FANCG gene that are known to cause the disease. Early detection through this genetic testing is crucial for managing the condition effectively. It allows for appropriate interventions and monitoring for potential complications associated with Fanconi anemia, such as leukemia and other cancers.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the FANCG Gene Fanconi Anemia Type G Genetic Test is available for a cost of 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetic analysis, ensuring accurate and reliable test results. This test is essential for families with a history of Fanconi anemia, as it can help in making informed decisions regarding treatment options and genetic counseling.

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  • This test is not intended for medical diagnosis or treatment
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FANCG Gene Fanconi Anemia Type G Genetic Test

Welcome to DNA Labs UAE, where we offer the FANCG Gene Fanconi anemia type G Genetic Test. This test is designed to diagnose individuals with Fanconi anemia type G, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer.

Test Details

The FANCG gene is associated with Fanconi anemia type G. Our Next-Generation Sequencing (NGS) technology allows for the simultaneous analysis of multiple genes, including the FANCG gene. By detecting variations or mutations in the FANCG gene, we can diagnose individuals with the condition, determine the inheritance pattern, and guide treatment decisions.

Components

  • Test Name: FANCG Gene Fanconi anemia type G Genetic Test
  • 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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to the FANCG Gene Fanconi anemia type G Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with Fanconi anemia type G.

Test Process

The NGS test involves obtaining a DNA sample, usually through a blood sample or saliva swab. The DNA is then sequenced using NGS technology to identify any variations or mutations in the FANCG gene. The results are interpreted by a geneticist or genetic counselor to provide a diagnosis or determine carrier status.

Conclusion

The FANCG Gene Fanconi anemia type G Genetic Test offered by DNA Labs UAE is an effective method for diagnosing individuals with Fanconi anemia type G. It provides valuable information about the condition, inheritance patterns, and treatment options. If you have a family history of this disorder or suspect that you may be affected, we encourage you to consider this test.

Test Name FANCG Gene Fanconi anemia type G 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FANCG Gene Fanconi anemia type G NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type G
Test Details

The FANCG gene is associated with Fanconi anemia type G, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the FANCG gene. NGS can detect variations or mutations in the FANCG gene that may be responsible for Fanconi anemia type G. This test can help diagnose individuals with the condition, determine the inheritance pattern, and guide treatment decisions. It can also be used for carrier testing in individuals with a family history of the disorder.

The NGS test involves obtaining a DNA sample, usually through a blood sample or saliva swab. The DNA is then sequenced using NGS technology to identify any variations or mutations in the FANCG gene. The results are interpreted by a geneticist or genetic counselor to provide a diagnosis or determine carrier status.

SKU: TEST-2310 Category:

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