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POLE Gene FILS Syndrome Genetic Test Cost

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

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The “POLE Gene FILS Syndrome Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the POLE gene that are associated with FILS syndrome. FILS syndrome is a rare genetic disorder characterized by facial dysmorphism, immunodeficiency, livedo, and short stature. The test aims to provide crucial genetic information that can help in the accurate diagnosis and management of the condition.

At DNA Labs UAE, the test is conducted with precision and care, ensuring reliable results. The cost of the test is set at 4400 AED, making it accessible to those who need it. This test is vital for families seeking answers about FILS syndrome, offering them a clear path towards understanding their genetic health and planning for any necessary treatments or interventions.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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POLE Gene FILS Syndrome Genetic Test

At DNA Labs UAE, we offer the POLE Gene FILS syndrome genetic test for individuals who suspect they may have this rare genetic disorder. This diagnostic test utilizes Next-Generation Sequencing (NGS) technology to analyze the POLE gene for mutations associated with FILS syndrome.

Test Details

The POLE gene FILS syndrome NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the POLE gene for mutations associated with FILS syndrome. FILS syndrome, also known as POLE-related syndrome, is a rare genetic disorder characterized by multiple colorectal adenomas and an increased risk of colorectal cancer. It is caused by mutations in the POLE gene, which encodes for the DNA polymerase epsilon enzyme involved in DNA replication and repair.

Components

  • Test Name: POLE Gene FILS syndrome Genetic Test
  • 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the POLE Gene FILS syndrome NGS genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by POLE Gene FILS syndrome NGS Genetic DNA Test gene POLE.

Benefits of the POLE Gene FILS Syndrome NGS Genetic Test

The NGS genetic test allows for a comprehensive assessment of genetic variants associated with FILS syndrome. It offers higher sensitivity and specificity compared to traditional genetic testing methods, enabling the detection of even rare mutations. The results of the test can help in genetic counseling, family planning, and personalized treatment decisions for individuals and families affected by FILS syndrome. Additionally, it may aid in identifying individuals at risk for developing colorectal cancer, enabling early detection and intervention.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. Our POLE Gene FILS syndrome NGS genetic test can provide valuable insights into an individual’s genetic makeup, allowing for better management and surveillance strategies for FILS syndrome.

Test Name POLE Gene FILS syndrome 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for POLE Gene FILS syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POLE Gene FILS syndrome NGS Genetic DNA Test gene POLE
Test Details

POLE gene FILS syndrome NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the POLE gene for mutations associated with FILS syndrome.

FILS syndrome, also known as POLE-related syndrome, is a rare genetic disorder characterized by multiple colorectal adenomas and an increased risk of colorectal cancer. It is caused by mutations in the POLE gene, which encodes for the DNA polymerase epsilon enzyme involved in DNA replication and repair.

The NGS genetic test involves sequencing the DNA of an individual to identify any alterations or mutations in the POLE gene. This can help in confirming a diagnosis of FILS syndrome and determining the appropriate management and surveillance strategies for the patient.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants associated with FILS syndrome. It offers higher sensitivity and specificity compared to traditional genetic testing methods, allowing for the detection of even rare mutations.

The results of the POLE gene FILS syndrome NGS genetic test can help in genetic counseling, family planning, and personalized treatment decisions for individuals and families affected by FILS syndrome. It may also aid in identifying individuals at risk for developing colorectal cancer, enabling early detection and intervention.

SKU: TEST-4112 Category:

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