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PNKP Gene Ataxia-Oculomotor Apraxia Type 4 Genetic Test

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

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The PNKP Gene Ataxia-Oculomotor Apraxia Type 4 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the PNKP gene associated with a rare neurological disorder. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that cause progressive ataxia and eye movement abnormalities. The test is essential for individuals experiencing coordination difficulties, involuntary eye movements, or those with a family history of neurological conditions. Results provide crucial information for accurate diagnosis, treatment planning, and genetic counseling. The test costs $500 USD and delivers results within 3-4 weeks using blood, extracted DNA, or blood spot samples. Early genetic testing enables proactive management strategies and informed family planning decisions.

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PNKP Gene Ataxia-Oculomotor Apraxia Type 4 NGS Genetic DNA Test

Comprehensive Introduction to PNKP Gene Testing

The PNKP Gene Ataxia-Oculomotor Apraxia Type 4 NGS Genetic DNA Test represents a significant advancement in neurological genetic diagnostics. This specialized test focuses on identifying mutations in the polynucleotide kinase 3′-phosphatase (PNKP) gene, which plays a crucial role in DNA repair mechanisms within nerve cells. When this gene malfunctions, it leads to progressive neurological deterioration characterized by coordination problems and abnormal eye movements. Early detection through genetic testing provides patients and healthcare providers with essential information for managing this rare hereditary condition effectively.

What This Advanced Test Detects

Our comprehensive NGS-based genetic analysis specifically targets:

  • Pathogenic variants in the PNKP gene associated with ataxia-oculomotor apraxia type 4
  • Single nucleotide polymorphisms (SNPs) affecting neurological function
  • Insertion and deletion mutations disrupting normal protein production
  • Genetic markers indicating increased risk for progressive neurological decline
  • Inheritance patterns that may affect family members

Who Should Consider PNKP Genetic Testing

Clinical Indications and Symptoms

This test is particularly recommended for individuals experiencing:

  • Progressive difficulty with coordination and balance (ataxia)
  • Abnormal involuntary eye movements (oculomotor apraxia)
  • Family history of neurological disorders or hereditary ataxia
  • Early-onset movement disorders without clear diagnosis
  • Developmental delays accompanied by motor coordination issues
  • Suspected autosomal recessive inheritance patterns in neurological conditions

Significant Benefits of Early Genetic Testing

Undergoing PNKP gene testing provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out specific genetic causes of neurological symptoms
  • Personalized Treatment Planning: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning Guidance: Provides crucial information for reproductive decisions
  • Proactive Management: Allows early intervention strategies to slow disease progression
  • Genetic Counseling Support: Facilitates comprehensive family risk assessment
  • Research Contribution: Helps advance understanding of rare neurological disorders

Understanding Your Test Results

Our genetic specialists provide detailed interpretation of your results:

  • Positive Result: Indicates presence of PNKP gene mutations; comprehensive genetic counseling recommended
  • Negative Result: Suggests absence of tested mutations; other neurological causes may need investigation
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Important information for family planning and genetic risk assessment

All results include detailed explanations and recommendations for next steps from our certified genetic counselors.

Test Pricing and Details

Test Feature Details
Test Name PNKP Gene Ataxia-Oculomotor Apraxia Type 4 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 serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, and many more. Our network of certified collection centers ensures accessible genetic testing services nationwide.

Take Control of Your Neurological Health Today

Don’t let uncertainty about neurological symptoms affect your quality of life. Our advanced PNKP genetic testing provides the clarity needed for proper diagnosis and management. Schedule your appointment now to begin your journey toward better neurological health management.

Call or WhatsApp us today at +1(267) 388-9828 to book your PNKP Gene Ataxia-Oculomotor Apraxia Type 4 NGS Genetic DNA Test and take the first step toward understanding your genetic health.