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NTF4 Gene Glaucoma Open Angle Type 1F Genetic Test

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

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The NTF4 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test is a cutting-edge genetic screening that identifies mutations in the NTF4 gene associated with hereditary open-angle glaucoma. This comprehensive test provides crucial information about genetic predisposition to glaucoma type 1F, enabling early intervention and personalized treatment strategies. Using advanced Next-Generation Sequencing (NGS) technology, the test delivers highly accurate results with a turnaround time of 3-4 weeks. The test is priced at $500 USD (discounted from $700) and is particularly valuable for individuals with family history of glaucoma or those experiencing early symptoms. Early genetic detection allows for proactive monitoring and preventive care to preserve vision and maintain optimal eye health.

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NTF4 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test

Understanding NTF4 Gene Glaucoma and Its Importance

The NTF4 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test represents a breakthrough in ophthalmological genetic testing, specifically designed to identify mutations in the Neurotrophin-4 (NTF4) gene associated with hereditary open-angle glaucoma. This progressive eye condition is characterized by increased intraocular pressure that damages the optic nerve, potentially leading to irreversible vision loss if left untreated. Early genetic detection through this advanced test enables proactive management strategies that can significantly delay disease progression and preserve visual function.

Glaucoma affects over 3 million Americans and is the second leading cause of blindness worldwide. The NTF4 gene plays a crucial role in retinal ganglion cell survival and optic nerve development, making mutations in this gene particularly significant for glaucoma risk assessment. Our comprehensive genetic analysis provides invaluable insights that traditional screening methods cannot offer, allowing for personalized treatment approaches based on individual genetic profiles.

What the Test Measures and Detects

This advanced genetic screening utilizes Next-Generation Sequencing (NGS) technology to comprehensively analyze the NTF4 gene for specific mutations linked to open-angle glaucoma type 1F. The test identifies:

  • Point mutations and single nucleotide polymorphisms (SNPs) in the NTF4 gene
  • Copy number variations affecting gene function
  • Specific pathogenic variants associated with increased glaucoma risk
  • Inheritance patterns that may affect family members
  • Genetic markers that influence treatment response and disease progression

The NGS methodology provides exceptional accuracy and coverage, ensuring comprehensive analysis of the entire NTF4 gene coding region and regulatory elements. This thorough approach minimizes the risk of false negatives and provides reliable genetic information for clinical decision-making.

Who Should Consider This Test

Primary Candidates for NTF4 Genetic Testing

  • Individuals with a family history of open-angle glaucoma, particularly among first-degree relatives
  • Patients experiencing early glaucoma symptoms such as gradual peripheral vision loss
  • Individuals with elevated intraocular pressure without apparent cause
  • Those with optic nerve abnormalities detected during routine eye examinations
  • Patients diagnosed with glaucoma at a young age (under 40 years)
  • Individuals from ethnic backgrounds with higher glaucoma prevalence

Symptoms and Risk Factors

  • Gradual loss of peripheral vision (tunnel vision)
  • Eye pain or discomfort
  • Halos around lights
  • Redness in the eyes
  • Nausea or vomiting (in acute cases)
  • Sudden vision disturbances
  • Family history of vision loss or blindness

Benefits of Taking the NTF4 Genetic Test

Early genetic testing for NTF4 mutations offers numerous advantages for proactive eye health management:

  • Early Risk Assessment: Identify genetic predisposition before symptoms develop, allowing for preventive measures
  • Personalized Treatment Plans: Tailor glaucoma management strategies based on individual genetic profiles
  • Family Planning Guidance: Understand inheritance patterns and risks for future generations
  • Reduced Healthcare Costs: Prevent expensive treatments through early intervention and monitoring
  • Peace of Mind: Clear genetic information reduces uncertainty and anxiety about glaucoma risk
  • Improved Monitoring: Establish appropriate screening frequency based on genetic risk factors
  • Treatment Optimization: Select medications and interventions most likely to be effective based on genetic markers

Understanding Your Test Results

Interpreting Genetic Findings

Your NTF4 genetic test results will fall into one of several categories, each with specific implications for your eye health management:

  • Positive Result: Indicates the presence of known pathogenic mutations in the NTF4 gene. This confirms increased genetic risk for open-angle glaucoma type 1F and warrants regular monitoring and preventive care.
  • Negative Result: No known pathogenic mutations detected. While this reduces genetic risk, regular eye examinations remain important as other genetic or environmental factors may contribute to glaucoma development.
  • Variant of Uncertain Significance (VUS): Identifies genetic changes with unknown clinical significance. These findings require careful interpretation by genetic counselors and ophthalmologists, with recommendations for continued monitoring.
  • Carrier Status: Important for family planning, as it indicates the potential to pass genetic mutations to offspring even without personal disease manifestation.

Next Steps After Testing

Following your genetic test results, our team provides comprehensive guidance including:

  • Detailed consultation with genetic counselors specializing in ophthalmological conditions
  • Referral to experienced ophthalmologists for ongoing care
  • Personalized monitoring schedule based on genetic risk assessment
  • Family screening recommendations when appropriate
  • Lifestyle and environmental risk factor management strategies

Test Information and Pricing

Test Component Details Price (USD)
Test Name NTF4 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test
Discount Price Limited Time Special Offer $500
Regular Price Standard Pricing $700
Turnaround Time Results Delivery 3-4 Weeks
Sample Type Collection Methods Blood, Extracted DNA, or Blood on FTA Card
Specialty Medical Discipline Ophthalmology Genetics
Testing Method Technology Used Next-Generation Sequencing (NGS)

Pre-Test Requirements and Preparation

To ensure optimal testing accuracy and comprehensive care, we require:

  • Complete clinical history documentation, including any existing eye conditions or symptoms
  • Genetic counseling session to discuss testing implications and create a family pedigree chart
  • Information about family members affected by glaucoma or vision disorders
  • Current medication list and relevant medical records
  • Informed consent understanding the benefits and limitations of genetic testing

Nationwide Availability and Booking

General Genetics Corporation provides comprehensive genetic testing services across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories and experienced genetic counselors ensure consistent, high-quality service regardless of location.

Take the first step toward proactive eye health management. Book your NTF4 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test today by calling our dedicated scheduling team at +1(267) 388-9828 or completing our online appointment request form. Early genetic detection could preserve your vision and transform your eye health future.

Our commitment to excellence in genetic testing extends beyond accurate results to comprehensive patient support, educational resources, and ongoing care coordination with your healthcare providers. Trust General Genetics Corporation for reliable, confidential, and clinically valuable genetic insights that empower informed healthcare decisions.