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TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test

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

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The TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the TUBB3 gene responsible for neurological development disorders. This comprehensive test utilizes next-generation sequencing technology to detect specific genetic variations that cause cortical dysplasia and associated brain malformations. Patients experiencing developmental delays, seizures, or neurological symptoms benefit from precise diagnosis and personalized treatment planning. The test provides crucial information for neurologists and genetic counselors to develop targeted intervention strategies. At $500 USD, this advanced genetic analysis offers affordable access to specialized neurological care. Results are typically available within 3-4 weeks from blood or DNA samples. Early genetic identification can significantly improve long-term neurological outcomes and family planning decisions.

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TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Development Disorders

The TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced testing method specifically targets mutations in the TUBB3 gene, which plays a critical role in brain development and neuronal migration. Cortical dysplasia complex with other brain malformations type 1 is a rare neurological condition characterized by abnormal brain structure development, often leading to significant neurological impairments and seizure disorders.

What This Test Measures and Detects

Our comprehensive NGS genetic test specifically analyzes:

  • TUBB3 gene mutations associated with cortical dysplasia
  • Genetic variations causing complex brain malformations
  • Specific nucleotide changes affecting microtubule function
  • Inheritance patterns for family genetic counseling
  • Risk assessment for neurological development disorders

The test utilizes next-generation sequencing technology to provide complete coverage of the TUBB3 gene, ensuring high accuracy in detecting even rare mutations that conventional testing might miss.

Who Should Consider This Genetic Test

This specialized genetic testing is recommended for individuals presenting with:

  • Unexplained developmental delays in infancy or childhood
  • Recurrent seizures or epilepsy of unknown origin
  • Abnormal brain imaging showing cortical malformations
  • Family history of neurological development disorders
  • Congenital brain abnormalities detected during pregnancy
  • Progressive neurological symptoms without clear diagnosis
  • Children with intellectual disabilities and motor impairments

Significant Benefits of TUBB3 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Precise Diagnosis: Obtain definitive genetic confirmation of cortical dysplasia complex
  • Personalized Treatment: Guide neurologists in developing targeted therapeutic approaches
  • Family Planning: Provide accurate genetic counseling for future pregnancies
  • Early Intervention: Enable timely implementation of developmental support services
  • Prognostic Information: Understand potential disease progression and outcomes
  • Research Contribution: Advance scientific understanding of neurological genetic disorders

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret your results:

  • Positive Result: Indicates presence of TUBB3 gene mutation; detailed counseling provided for management strategies
  • Negative Result: Suggests absence of tested mutations; may require additional neurological evaluation
  • Variant of Uncertain Significance: Identifies genetic changes requiring further research and monitoring
  • Carrier Status: Important information for family planning and genetic counseling

All results include detailed explanations from our certified genetic counselors, ensuring you fully understand the implications for your neurological health and family planning decisions.

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700

Turnaround Time: 3 to 4 Weeks
Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card

Nationwide Testing Availability

We provide comprehensive genetic testing services across the United States with convenient locations in all major cities 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 testing for patients nationwide.

Pre-Test Requirements

To ensure optimal testing outcomes, we recommend:

  • Complete clinical history documentation
  • Genetic counseling session for comprehensive family pedigree analysis
  • Neurological evaluation and imaging results when available
  • Informed consent understanding the test implications

Take Control of Your Neurological Health Today

Don’t let unexplained neurological symptoms remain a mystery. Our TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 NGS Genetic DNA Test provides the answers you need for proper diagnosis and treatment planning. With our advanced genetic testing technology and expert neurological genetics team, you can make informed decisions about your health care journey.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward understanding your neurological health.

Our dedicated team of genetic specialists and neurologists are committed to providing comprehensive care and support throughout your testing journey. Early genetic diagnosis can significantly impact treatment outcomes and quality of life for individuals with cortical dysplasia and associated brain malformations.