FANCL Gene Fanconi anemia type L Genetic Test
Welcome to DNA Labs UAE, where we offer the FANCL Gene Fanconi anemia type L Genetic Test. This test aims to analyze the FANCL gene for mutations associated with Fanconi anemia type L.
Test Details
The FANCL Gene Fanconi anemia type L NGS Genetic Test is a genetic test that analyzes the FANCL gene for mutations associated with Fanconi anemia type L. Fanconi anemia is a rare genetic disorder that affects the body’s ability to repair damaged DNA, leading to bone marrow failure, birth defects, and an increased risk of cancer.
The FANCL gene is one of several genes associated with Fanconi anemia, and mutations in this gene can cause Fanconi anemia type L. NGS (Next-Generation Sequencing) technology is used in this test to analyze the entire coding region of the FANCL gene, allowing for the detection of various types of mutations, including small insertions, deletions, and single nucleotide variants.
By identifying mutations in the FANCL gene, this test can help diagnose Fanconi anemia type L and provide important information for genetic counseling and family planning.
Test Components and Price
The FANCL Gene Fanconi anemia type L Genetic Test is priced at 4400.0 AED. The test can be conducted using blood or extracted DNA, or even just one drop of blood on an FTA card.
Report Delivery and Method
After conducting the test, the report will be delivered within 3 to 4 weeks. The NGS technology is utilized in this test for accurate and efficient analysis.
Test Type and Doctor
The FANCL Gene Fanconi anemia type L Genetic Test falls under the category of Metabolic Disorders. It is recommended to consult a General Physician for this test.
Test Department
This test is conducted in our Genetics department, where our team of experts ensures accurate and reliable results.
Pre Test Information
Before conducting the FANCL Gene Fanconi anemia type L NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected with Fanconi anemia type L.
Important Considerations
It is important to note that this test specifically targets mutations in the FANCL gene and does not analyze other genes associated with Fanconi anemia. Additionally, a negative test result does not completely rule out the possibility of having Fanconi anemia, as there may be mutations in other genes not tested for. Therefore, a comprehensive evaluation by a healthcare professional is necessary for an accurate diagnosis.
| Test Name | FANCL Gene Fanconi anemia type L 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 FANCL Gene Fanconi anemia type L NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type L |
| Test Details |
The FANCL Gene Fanconi anemia type L NGS Genetic Test is a genetic test that analyzes the FANCL gene for mutations associated with Fanconi anemia type L. Fanconi anemia is a rare genetic disorder that affects the body’s ability to repair damaged DNA, leading to bone marrow failure, birth defects, and an increased risk of cancer. The FANCL gene is one of several genes associated with Fanconi anemia, and mutations in this gene can cause Fanconi anemia type L. NGS (Next-Generation Sequencing) technology is used in this test to analyze the entire coding region of the FANCL gene, allowing for the detection of various types of mutations, including small insertions, deletions, and single nucleotide variants. By identifying mutations in the FANCL gene, this test can help diagnose Fanconi anemia type L and provide important information for genetic counseling and family planning. It is important to note that this test specifically targets mutations in the FANCL gene and does not analyze other genes associated with Fanconi anemia. Additionally, a negative test result does not completely rule out the possibility of having Fanconi anemia, as there may be mutations in other genes not tested for. Therefore, a comprehensive evaluation by a healthcare professional is necessary for an accurate diagnosis. |
