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SLX4 Gene Fanconi anemia type P Genetic Test Cost

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

-21%

The SLX4 gene plays a critical role in DNA repair mechanisms and is closely associated with Fanconi anemia type P, a rare genetic disorder. This condition can lead to various physical abnormalities, bone marrow failure, and increased cancer risk. Identifying mutations in the SLX4 gene is crucial for diagnosing Fanconi anemia type P, enabling early intervention and management of the condition.

DNA Labs UAE offers a specialized genetic test targeting the SLX4 gene to identify mutations linked to Fanconi anemia type P. The test is conducted with high precision, ensuring reliable results for patients and their families. With a cost of 4400 AED, the test is an investment in understanding and managing this genetic condition more effectively. By opting for this test, individuals can gain insights into their genetic makeup, leading to informed decisions regarding their health and the possibility of passing the condition to future generations.

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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.

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