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FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 Genetic Test

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

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The FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 NGS Genetic DNA Test is a cutting-edge genetic diagnostic tool that identifies mutations in the FYCO1 gene responsible for congenital cataracts. This comprehensive test utilizes Next Generation Sequencing technology to provide accurate detection of autosomal recessive inherited eye conditions. For individuals with family history of congenital cataracts or early-onset vision problems, this test offers crucial diagnostic information for treatment planning and genetic counseling. The test requires a simple blood sample or extracted DNA and delivers results within 3-4 weeks. Priced at $500 USD, this advanced genetic analysis helps families understand their hereditary risk factors and make informed healthcare decisions.

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FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 NGS Genetic DNA Test

Comprehensive Genetic Testing for Inherited Cataract Conditions

The FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 NGS Genetic DNA Test represents a breakthrough in ophthalmic genetic diagnostics, providing families with crucial insights into hereditary vision disorders. This advanced genetic analysis specifically targets mutations in the FYCO1 gene, which plays a critical role in lens development and transparency. Congenital cataracts affecting infants and young children can significantly impact visual development, making early detection and intervention essential for optimal outcomes.

What Does This Test Measure and Detect?

This sophisticated genetic test utilizes Next Generation Sequencing (NGS) technology to comprehensively analyze the FYCO1 gene for pathogenic variants associated with autosomal recessive congenital cataracts type 2. The test specifically identifies:

  • Point mutations, deletions, and insertions in the FYCO1 gene
  • Autosomal recessive inheritance patterns
  • Genetic variants affecting lens protein structure and function
  • Mutations that disrupt normal lens development during embryogenesis
  • Specific genetic markers linked to congenital cataract formation

Who Should Consider This Genetic Test?

This specialized genetic analysis is recommended for individuals and families experiencing:

  • Infants or children with congenital cataracts present at birth or developing in early childhood
  • Family history of inherited cataract disorders across multiple generations
  • Parents planning pregnancy with known family history of congenital eye conditions
  • Individuals with unexplained vision problems despite normal eye examinations
  • Patients requiring precise diagnosis for targeted treatment planning
  • Couples seeking preconception genetic counseling for hereditary eye disorders

Clinical Symptoms and Indications

Early recognition of symptoms associated with FYCO1 gene mutations is crucial for timely intervention. Common clinical presentations include:

  • Cloudy or opaque lens appearance in newborns
  • Progressive vision deterioration in early childhood
  • Nystagmus (involuntary eye movements)
  • Strabismus (misaligned eyes)
  • Photophobia (light sensitivity)
  • Delayed visual developmental milestones
  • Family clustering of cataract cases

Benefits of FYCO1 Genetic Testing

Early Intervention and Treatment Planning

Genetic confirmation enables ophthalmologists to develop targeted treatment strategies, including timely surgical interventions when necessary. Early diagnosis facilitates:

  • Precise timing for cataract surgery to optimize visual outcomes
  • Customized visual rehabilitation programs
  • Appropriate prescription of corrective lenses
  • Monitoring for associated ocular complications

Family Planning and Genetic Counseling

The autosomal recessive nature of this condition means both parents must carry the gene mutation for a child to be affected. Genetic testing provides:

  • Accurate recurrence risk assessment for future pregnancies
  • Informed reproductive decision-making
  • Comprehensive family pedigree analysis
  • Access to specialized genetic counseling services

Personalized Medical Management

Understanding your specific genetic profile allows healthcare providers to:

  • Tailor monitoring schedules based on genetic risk
  • Implement preventive measures for optimal eye health
  • Coordinate care with multiple specialists when needed
  • Provide evidence-based prognostic information

Understanding Your Test Results

Positive Result Interpretation

A positive result indicates the presence of pathogenic mutations in the FYCO1 gene associated with autosomal recessive congenital cataracts. This confirmation enables:

  • Definitive diagnosis and appropriate medical management
  • Family member testing and cascade screening
  • Access to specialized ophthalmic care and resources
  • Eligibility for clinical trials and research studies

Negative Result Implications

A negative result suggests that no pathogenic FYCO1 gene mutations were detected. However, this does not completely rule out other genetic causes of congenital cataracts. Further evaluation may include:

  • Testing for other cataract-associated genes
  • Comprehensive ophthalmological examination
  • Consideration of non-genetic cataract causes
  • Continued monitoring for visual development

Variant of Uncertain Significance (VUS)

In some cases, genetic variants of unknown clinical significance may be identified. Our genetic counseling team provides:

  • Detailed explanation of variant implications
  • Recommendations for family studies
  • Guidance on ongoing research and variant reclassification
  • Support for clinical decision-making

Test Details and Pricing

Test Component Details
Test Name FYCO1 Gene Cataract Autosomal Recessive Congenital Type 2 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
Medical Specialty Ophthalmology Genetics

Pre-Test Requirements and Preparation

To ensure accurate results and comprehensive care, we require:

  • Complete clinical history of the patient undergoing testing
  • Genetic counseling session to create detailed family pedigree
  • Documentation of affected family members with similar conditions
  • Informed consent for genetic testing and result disclosure
  • Insurance information and payment arrangements

Nationwide Accessibility and Convenience

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection centers ensures accessible genetic testing services for families nationwide.

Take Control of Your Genetic Health Today

Don’t let uncertainty about hereditary eye conditions affect your family’s future. Our FYCO1 Gene Cataract NGS Genetic DNA Test provides the clarity and confidence you need for informed healthcare decisions. With our discounted price of $500 USD and comprehensive genetic counseling support, you can access world-class genetic diagnostics without financial burden.

Ready to schedule your genetic test? Contact our dedicated genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and guide you through the testing process with compassion and expertise.

Take the first step toward understanding your genetic heritage and protecting your family’s visual health. Early detection through advanced genetic testing can make a significant difference in treatment outcomes and quality of life.