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FANCB Gene Fanconi anemia type B Genetic Test Cost

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

-21%

The “FANCB Gene Fanconi Anemia Type B Genetic Test” is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the FANCB gene, which are responsible for Fanconi anemia type B. Fanconi anemia is a rare genetic disorder that leads to bone marrow failure and increased risk of cancer. The FANCB gene plays a crucial role in the body’s ability to repair DNA damage, and mutations in this gene can disrupt this process, leading to the development of the disease.

This test is particularly important for individuals with a family history of Fanconi anemia or those presenting symptoms related to the condition, such as physical abnormalities, bone marrow failure, or early onset of cancers. Early detection through the FANCB gene test can facilitate timely intervention and management of the disease, potentially improving the quality of life and survival rates of affected individuals.

DNA Labs UAE offers this test at a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for any mutations in the FANCB gene. Results from this test can provide crucial information for families regarding the risk of Fanconi anemia in current or future offspring and can guide decisions regarding genetic counseling and management strategies for the condition.

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FANCB Gene Fanconi Anemia Type B Genetic Test

Are you concerned about Fanconi anemia type B? DNA Labs UAE offers a comprehensive genetic test that can provide valuable insights into this rare genetic disorder. In this blog, we will discuss the symptoms, diagnosis, and cost of the FANCB Gene Fanconi anemia type B Genetic Test.

Test Name: FANCB Gene Fanconi Anemia Type B 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

Before undergoing the FANCB Gene Fanconi anemia type B 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 Fanconi anemia type B.

Test Details

The FANCB gene is associated with Fanconi anemia type B, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of certain cancers. The NGS (Next-Generation Sequencing) genetic testing method allows for the analysis of multiple genes simultaneously.

In the context of Fanconi anemia type B, the NGS genetic test will specifically sequence the FANCB gene to identify any mutations or variations that may be present. This test can help diagnose individuals suspected of having Fanconi anemia type B and identify carriers of the FANCB gene mutation. It can also be used for prenatal testing in families with a known FANCB gene mutation to determine if a fetus is affected.

Genetic testing for Fanconi anemia type B provides valuable information for healthcare providers, individuals, and families. It aids in early diagnosis, appropriate medical management, and family planning decisions. However, it is important to consult with a healthcare professional or genetic counselor to fully understand the implications and limitations of the test results.

Don’t wait, take control of your health and get tested for Fanconi anemia type B today. Contact DNA Labs UAE to schedule your genetic test.

Test Name FANCB Gene Fanconi anemia type B 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 FANCB Gene Fanconi anemia type B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type B
Test Details

The FANCB gene is associated with Fanconi anemia type B, a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of certain cancers.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Fanconi anemia type B, an NGS genetic test would involve sequencing the FANCB gene to identify any mutations or variations that may be present.

The NGS test for Fanconi anemia type B can help diagnose individuals suspected of having this condition and also identify carriers of the FANCB gene mutation. It can also be used for prenatal testing in families with a known FANCB gene mutation to determine if a fetus is affected.

Genetic testing for Fanconi anemia type B can provide valuable information for healthcare providers, individuals, and families. It can aid in early diagnosis, appropriate medical management, and family planning decisions. However, it is important to consult with a healthcare professional or genetic counselor to understand the implications and limitations of the test results.

SKU: TEST-2305