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CP Gene Cerebellar Ataxia Genetic Test

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

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The CP Gene Cerebellar Ataxia NGS Genetic DNA Test is a comprehensive diagnostic tool that utilizes Next Generation Sequencing technology to identify mutations in the CP gene associated with hereditary cerebellar ataxia. This advanced genetic test helps diagnose individuals experiencing progressive coordination difficulties, gait abnormalities, and neurological symptoms. By analyzing specific genetic markers, the test provides crucial information for accurate diagnosis, treatment planning, and family risk assessment. The test is particularly valuable for patients with unexplained neurological symptoms, family history of ataxia, or those seeking genetic counseling. Results are typically available within 3-4 weeks, and the test requires a simple blood sample or extracted DNA. At only $500 USD, this test offers accessible advanced genetic diagnostics for neurological conditions across our nationwide network of testing centers.

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CP Gene Cerebellar Ataxia NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Cerebellar Ataxia

The CP Gene Cerebellar Ataxia NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for hereditary cerebellar ataxia disorders. This advanced testing methodology utilizes cutting-edge Next Generation Sequencing (NGS) technology to provide comprehensive analysis of the CP gene, enabling accurate diagnosis and personalized treatment approaches for patients experiencing progressive coordination difficulties.

What Does This Test Measure and Detect?

This sophisticated genetic test specifically targets and analyzes the CP gene, which plays a crucial role in neurological function and coordination. The test detects:

  • Pathogenic mutations in the CP gene associated with cerebellar ataxia
  • Single nucleotide variants (SNVs) and small insertions/deletions
  • Genetic markers indicating hereditary ataxia predisposition
  • Specific mutation types that influence disease progression and severity
  • Carrier status for family planning purposes

Using NGS technology, the test provides comprehensive coverage of the entire CP gene coding region, ensuring no significant mutations are missed during analysis.

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals experiencing:

  • Progressive coordination difficulties and balance problems
  • Unexplained gait abnormalities or walking difficulties
  • Family history of cerebellar ataxia or similar neurological disorders
  • Speech difficulties or slurred speech development
  • Eye movement abnormalities or nystagmus
  • Muscle stiffness or spasticity without clear cause
  • Developmental delays in motor skills
  • Planning pregnancy with family history of neurological conditions

Significant Benefits of Genetic Testing

Undergoing the CP Gene Cerebellar Ataxia NGS Genetic DNA Test provides numerous advantages:

  • Accurate Diagnosis: Provides definitive answers for unexplained neurological symptoms
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Offers crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates timely management strategies to slow disease progression
  • Risk Assessment: Identifies at-risk family members for proactive monitoring
  • Peace of Mind: Reduces uncertainty and provides clarity about neurological health

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of neurological genetics specialists:

  • Positive Result: Indicates the presence of a pathogenic mutation in the CP gene, confirming hereditary cerebellar ataxia diagnosis
  • Negative Result: Suggests no detectable mutations in the CP gene, though other genetic or non-genetic causes should be considered
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications, requiring further evaluation
  • Carrier Status: Determines if you carry a single copy of a mutation that could be passed to offspring

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps for medical management.

Test Pricing and Details

Test Component Details
Test Name CP Gene Cerebellar Ataxia 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

Nationwide Testing Availability

We proudly offer comprehensive genetic testing services across the United States, with convenient locations in all 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 certified genetic counselors ensure consistent, high-quality testing standards nationwide.

Take Control of Your Neurological Health Today

Don’t let uncertainty about neurological symptoms affect your quality of life. The CP Gene Cerebellar Ataxia NGS Genetic DNA Test provides the clarity and answers you need for proper diagnosis and treatment planning. Our team of neurological genetics specialists is ready to guide you through the testing process and help interpret your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Take the first step toward understanding your neurological health with confidence and precision.