Sale!

FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease FKRP Related Genetic Test

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

-29%

The FKRP Gene Walker-Warburg Syndrome NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the FKRP gene associated with Walker-Warburg syndrome and muscle-eye-brain disease. This advanced next-generation sequencing test provides crucial genetic information for patients experiencing neurological symptoms, muscle weakness, and developmental delays. The test helps confirm diagnosis, guide treatment decisions, and provide valuable information for family planning. Available for $500 USD, this specialized genetic analysis offers precise detection of FKRP gene variants that cause these rare congenital muscular dystrophies. Early genetic testing can significantly impact patient management and improve long-term outcomes.

Trusted Testing. Expert Care. Guaranteed Privacy.

  • Accredited and Trusted
  • Expert Scientists, Advanced Technology
  • Data Privacy Guaranteed
Guaranteed Safe Checkout

FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease FKRP Related NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Neurological Disorders

The FKRP Gene Walker-Warburg Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the FKRP (Fukutin-Related Protein) gene, which plays a critical role in muscle and brain development. This specialized genetic test utilizes next-generation sequencing technology to provide comprehensive analysis of the FKRP gene, enabling accurate diagnosis of Walker-Warburg syndrome and related muscle-eye-brain diseases.

What This Advanced Genetic Test Detects

Our NGS-based FKRP gene test specifically identifies:

  • Pathogenic variants in the FKRP gene associated with congenital muscular dystrophies
  • Mutations causing Walker-Warburg syndrome, a severe form of congenital muscular dystrophy
  • Genetic alterations linked to muscle-eye-brain disease spectrum disorders
  • Both inherited and de novo mutations affecting alpha-dystroglycan glycosylation
  • Specific genetic markers that help differentiate between related neurological conditions

Who Should Consider FKRP Genetic Testing?

Clinical Indications and Symptoms

This specialized genetic test is recommended for individuals presenting with:

  • Congenital muscular weakness and hypotonia (low muscle tone)
  • Developmental delays in motor milestones
  • Brain abnormalities detected on MRI, particularly cobblestone lissencephaly
  • Ocular abnormalities including retinal dysplasia, microphthalmia, or congenital cataracts
  • Family history of Walker-Warburg syndrome or related congenital muscular dystrophies
  • Unexplained neurological symptoms in infancy or early childhood
  • Suspected alpha-dystroglycanopathies based on clinical presentation

Significant Benefits of FKRP Genetic Testing

Transformative Diagnostic Advantages

Undergoing FKRP gene testing provides numerous critical benefits:

  • Accurate Diagnosis: Confirms or rules out Walker-Warburg syndrome and related disorders
  • Personalized Treatment Planning: Enables targeted management strategies based on genetic findings
  • Family Planning Guidance: Provides essential information for genetic counseling and reproductive decisions
  • Prognostic Information: Helps predict disease progression and potential complications
  • Early Intervention: Facilitates timely implementation of supportive therapies and interventions
  • Research Contribution: Advances understanding of rare neurological disorders

Understanding Your Genetic Test Results

Comprehensive Result Interpretation

Our genetic specialists provide detailed analysis of your FKRP gene test results:

  • Positive Result: Identification of pathogenic FKRP variants confirms diagnosis and guides management
  • Negative Result: Absence of detected mutations may suggest alternative diagnoses
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Identifies individuals at risk of passing mutations to offspring

All results include comprehensive genetic counseling to ensure proper understanding and next steps.

Test Information and Pricing

Test Component Details
Test Name FKRP Gene Walker-Warburg Syndrome or Muscle-Eye-Brain Disease FKRP Related NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 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 Neurology and Genetics

Nationwide Testing Availability

We proudly offer 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 network of certified genetic counselors and specialized neurologists ensures you receive expert care regardless of your location.

Take Control of Your Genetic Health Today

Don’t let uncertainty about neurological symptoms delay your path to accurate diagnosis and appropriate care. Our FKRP Gene NGS Test provides the definitive genetic information needed to make informed healthcare decisions. With our discounted price of $500 USD and comprehensive genetic counseling support, you can access world-class diagnostic testing without financial burden.

Ready to schedule your genetic test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your genetic health and securing the specialized care you deserve.