SLX4 Gene Fanconi Anemia Type P Genetic Test
At DNA Labs UAE, we offer the SLX4 Gene Fanconi Anemia Type P Genetic Test. This test is designed to detect mutations or variations in the SLX4 gene, which is associated with Fanconi anemia type P. Fanconi anemia type P is a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer.
Test Details
The SLX4 Gene Fanconi Anemia Type P Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This provides a comprehensive assessment of an individual’s genetic makeup. In the case of Fanconi anemia type P, this test specifically focuses on the SLX4 gene.
Test Components and Price
The SLX4 Gene Fanconi Anemia Type P Genetic Test costs AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA Card. The report will be delivered within 3 to 4 weeks.
Test Type and Department
The SLX4 Gene Fanconi Anemia Type P Genetic Test falls under the category of Metabolic Disorders. It is conducted by our Genetics department.
Doctor and Pre Test Information
A General Physician will oversee the SLX4 Gene Fanconi Anemia Type P Genetic Test. Before the test, a Genetic Counselling session will be conducted to gather the clinical history of the patient. This session will also involve drawing a pedigree chart of family members affected by Fanconi anemia type P.
Importance of Genetic Testing
Genetic testing is a crucial tool for diagnostic purposes, genetic counseling, and potentially guiding treatment decisions. It is important to note that genetic testing should be performed by a qualified healthcare professional who specializes in genetics. The interpretation of test results can be complex and requires expertise in the field. Additionally, genetic testing may not be necessary or appropriate for every individual. Therefore, it is essential to consult with a healthcare professional to determine if the SLX4 Gene Fanconi Anemia Type P Genetic Test is appropriate for a given situation.
| Test Name | SLX4 Gene Fanconi anemia type P 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 SLX4 Gene Fanconi anemia type P NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type P |
| Test Details |
The SLX4 gene is associated with Fanconi anemia type P, which is a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of Fanconi anemia type P, NGS genetic testing can be used to identify mutations or variations in the SLX4 gene that may be responsible for the condition. By analyzing the SLX4 gene using NGS technology, healthcare professionals can determine if an individual has any mutations or variations that are associated with Fanconi anemia type P. This information can be used for diagnostic purposes, genetic counseling, and potentially guiding treatment decisions. It is important to note that genetic testing should be performed by a qualified healthcare professional who specializes in genetics, as the interpretation of test results can be complex and require expertise in the field. Additionally, genetic testing may not be necessary or appropriate for every individual, so it is important to consult with a healthcare professional to determine if it is appropriate in a given situation. |
