XRCC2 Gene Fanconi anemia XRCCR2 related Genetic Test
At DNA Labs UAE, we offer the XRCC2 Gene Fanconi anemia XRCCR2 related Genetic Test. This test is designed to analyze the XRCC2 gene, which is involved in the repair of damaged DNA.
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 XRCC2 Gene Fanconi anemia, XRCCR2 related NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia, XRCCR2 related
Test Details
The XRCC2 gene is involved in the repair of damaged DNA. Mutations in this gene can lead to a condition called Fanconi anemia, which is a rare genetic disorder characterized by bone marrow failure, birth defects, and an increased risk of cancer.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a particular condition. In the case of XRCC2-related Fanconi anemia, NGS genetic testing can be used to identify mutations or variations in the XRCC2 gene that may be causing the disorder.
NGS genetic testing typically involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the DNA to identify any mutations or variations. This information can then be used to diagnose the condition, determine the risk of developing related health problems, and guide treatment options.
It is important to note that genetic testing for XRCC2-related Fanconi anemia is typically done in specialized laboratories and should be ordered by a healthcare professional who specializes in genetics. The results of the genetic test should be interpreted by a genetic counselor or geneticist who can provide appropriate counseling and guidance based on the individual’s specific genetic profile.
| Test Name | XRCC2 Gene Fanconi anemia XRCCR2 related 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 XRCC2 Gene Fanconi anemia, XRCCR2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia, XRCCR2 related |
| Test Details | The XRCC2 gene is involved in the repair of damaged DNA. Mutations in this gene can lead to a condition called Fanconi anemia, which is a rare genetic disorder characterized by bone marrow failure, birth defects, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a particular condition. In the case of XRCC2-related Fanconi anemia, NGS genetic testing can be used to identify mutations or variations in the XRCC2 gene that may be causing the disorder. NGS genetic testing typically involves obtaining a DNA sample, usually through a blood or saliva sample, and then sequencing the DNA to identify any mutations or variations. This information can then be used to diagnose the condition, determine the risk of developing related health problems, and guide treatment options. It is important to note that genetic testing for XRCC2-related Fanconi anemia is typically done in specialized laboratories and should be ordered by a healthcare professional who specializes in genetics. The results of the genetic test should be interpreted by a genetic counselor or geneticist who can provide appropriate counseling and guidance based on the individual’s specific genetic profile. |
