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FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa Genetic Test

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

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The FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the FLVCR1 gene responsible for a rare inherited neurological disorder. This comprehensive test utilizes Next Generation Sequencing technology to detect specific genetic variations that cause progressive ataxia, posterior column degeneration, and retinitis pigmentosa. Early detection through this test enables proactive management strategies and personalized treatment approaches. The test is particularly valuable for individuals experiencing coordination difficulties, vision problems, or those with family history of neurological conditions. At just $500 USD, this advanced genetic analysis provides crucial insights for patients and healthcare providers in managing complex neurological disorders effectively.

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FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This specialized test focuses on identifying mutations in the FLVCR1 gene, which plays a critical role in cellular heme transport and mitochondrial function. When this gene malfunctions, it leads to a complex neurological condition characterized by progressive ataxia, degeneration of the posterior columns in the spinal cord, and retinitis pigmentosa affecting vision.

What This Advanced Test Detects

Our NGS Genetic DNA Test specifically targets:

  • Pathogenic variants in the FLVCR1 gene responsible for neurological symptoms
  • Specific mutations affecting heme transport and cellular metabolism
  • Genetic markers associated with progressive ataxia and coordination issues
  • Variants linked to posterior column degeneration affecting sensory function
  • Genetic factors contributing to retinitis pigmentosa and vision impairment

Who Should Consider This Genetic Test?

This comprehensive genetic analysis is recommended for individuals experiencing:

  • Progressive coordination difficulties and balance problems
  • Family history of inherited neurological disorders
  • Unexplained vision changes or night blindness
  • Sensory abnormalities in limbs and extremities
  • Early-onset neurological symptoms with unclear diagnosis
  • Multiple family members affected by similar neurological conditions

Clinical Indications and Symptoms

Patients presenting with the following symptoms should consider this test:

  • Difficulty with coordination and balance (ataxia)
  • Progressive vision loss, particularly night blindness
  • Sensory impairment in hands and feet
  • Muscle weakness and fatigue
  • Family history of retinitis pigmentosa
  • Neurological symptoms beginning in childhood or early adulthood

Significant Benefits of Genetic Testing

Undergoing the FLVCR1 Gene Test provides numerous advantages:

  • Accurate Diagnosis: Provides definitive identification of the genetic cause of symptoms
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Offers crucial information for genetic counseling and family planning decisions
  • Early Intervention: Facilitates proactive management strategies before significant disability develops
  • Peace of Mind: Reduces diagnostic uncertainty and provides clear direction for care
  • Research Contribution: Helps advance understanding of rare neurological disorders

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret results:

  • Positive Result: Indicates presence of FLVCR1 gene mutation; enables targeted management and family screening
  • Negative Result: Suggests symptoms may have other causes; guides further diagnostic evaluation
  • Variant of Uncertain Significance: Requires additional family studies and ongoing monitoring
  • Carrier Status: Important information for family planning and genetic counseling

Test Pricing and Availability

Test Name Regular Price Discount Price
FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa NGS Genetic DNA Test $700 USD $500 USD

Nationwide Testing Availability

We have convenient testing locations across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.

Take Control of Your Neurological Health

Don’t let uncertainty about your neurological symptoms delay proper diagnosis and treatment. Our FLVCR1 Gene Test provides the clarity needed to make informed healthcare decisions. With results available in 3-4 weeks and comprehensive genetic counseling support, you’ll have the information necessary to work with your neurologist on an effective management plan.

Ready to take the next step? Book your FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa NGS Genetic DNA Test today by calling our genetic specialists at +1(267) 388-9828 or schedule your appointment online. Early detection leads to better outcomes – take control of your neurological health now.