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POLE Gene FILS Syndrome NGS Genetic DNA Test

Original price was: $700.Current price is: $500.

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The POLE Gene FILS Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the POLE gene associated with Facial Dysmorphism, Intellectual Disability, and Limb Abnormalities Syndrome. This advanced next-generation sequencing test provides crucial diagnostic information for individuals presenting with developmental delays, distinctive facial features, and skeletal anomalies. By detecting specific genetic variants, the test enables accurate diagnosis, facilitates personalized treatment approaches, and helps families understand inheritance patterns. Available for $500 USD, this test offers significant clinical value for pediatric patients and individuals with suspected genetic disorders affecting multiple body systems. Early genetic diagnosis can guide appropriate medical management and provide valuable information for family planning decisions.

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POLE Gene FILS Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for Developmental Disorders

The POLE Gene FILS Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic tool designed to identify mutations in the POLE gene, which are responsible for Facial Dysmorphism, Intellectual Disability, and Limb Abnormalities Syndrome (FILS). This comprehensive genetic analysis utilizes next-generation sequencing technology to provide accurate and reliable results for individuals and families affected by this complex developmental disorder.

What Does This Test Measure and Detect?

This advanced genetic test specifically targets the POLE gene, which encodes the catalytic subunit of DNA polymerase epsilon. The test detects:

  • Pathogenic variants and mutations in the POLE gene
  • Single nucleotide variants (SNVs) associated with FILS syndrome
  • Small insertions and deletions affecting gene function
  • Genetic changes that disrupt normal DNA replication and repair mechanisms

The NGS technology employed in this test provides comprehensive coverage of the entire POLE gene, ensuring high sensitivity and specificity in mutation detection.

Who Should Consider This Test?

This genetic test is particularly recommended for individuals presenting with the following symptoms and clinical features:

  • Children with developmental delays and intellectual disability
  • Individuals with distinctive facial dysmorphism including prominent forehead, deep-set eyes, and abnormal ear placement
  • Patients with limb abnormalities such as syndactyly, brachydactyly, or other skeletal anomalies
  • Families with a history of similar developmental disorders
  • Individuals with growth retardation and microcephaly
  • Patients with multiple congenital anomalies affecting different body systems

Clinical Benefits of Genetic Testing

Undergoing the POLE Gene FILS Syndrome NGS Genetic DNA Test offers numerous advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation of FILS syndrome
  • Personalized Treatment Planning: Enables targeted medical management and intervention strategies
  • Family Planning Guidance: Offers valuable information for reproductive decision-making
  • Early Intervention: Facilitates timely implementation of developmental therapies
  • Genetic Counseling: Supports families in understanding inheritance patterns and recurrence risks
  • Research Contribution: Helps advance scientific understanding of rare genetic disorders

Understanding Your Test Results

Your genetic test results will be carefully analyzed and interpreted by our team of certified genetic counselors and medical geneticists. The report will include:

  • Detailed explanation of identified genetic variants
  • Clinical significance of detected mutations
  • Inheritance pattern information
  • Recommendations for medical follow-up and management
  • Family testing considerations
  • Access to genetic counseling services for result interpretation

Positive results confirming POLE gene mutations provide definitive diagnosis, while negative results may help exclude FILS syndrome and guide further diagnostic evaluation.

Test Information and Pricing

Test Component Details
Test Name POLE Gene FILS Syndrome NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology
Specialty Pediatric Genetics

Pre-Test Requirements

Before undergoing testing, patients should provide:

  • Complete clinical history and symptom documentation
  • Participation in a genetic counseling session
  • Development of a detailed pedigree chart documenting family members affected by similar conditions
  • Informed consent for genetic testing

Nationwide Testing Availability

We proudly offer the POLE Gene FILS Syndrome NGS Genetic DNA Test across the United States, with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our nationwide network ensures accessible genetic testing services for patients throughout the country.

Take the Next Step Toward Genetic Clarity

If you or your loved one is experiencing symptoms suggestive of FILS syndrome or related developmental disorders, don’t wait to seek genetic answers. Our comprehensive POLE Gene NGS test provides the clarity needed for proper diagnosis and management.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our dedicated team is ready to assist you with the testing process and answer any questions you may have about POLE gene testing and FILS syndrome.

Early genetic diagnosis can make a significant difference in treatment outcomes and quality of life. Take control of your genetic health journey with our advanced NGS testing services.