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TUBB2B Gene Polymicrogyria Asymmetric NGS Genetic DNA Test

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

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The TUBB2B Gene Polymicrogyria Asymmetric NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the TUBB2B gene associated with asymmetric polymicrogyria, a rare brain malformation disorder. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variations that affect brain development during pregnancy. The test is crucial for individuals showing neurological symptoms, developmental delays, or family history of brain malformations. Results help guide treatment decisions, provide prognostic information, and facilitate genetic counseling for family planning. The test costs $500 USD and provides results within 3-4 weeks using blood or DNA samples.

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TUBB2B Gene Polymicrogyria Asymmetric NGS Genetic DNA Test

Comprehensive Genetic Testing for Brain Development Disorders

The TUBB2B Gene Polymicrogyria Asymmetric NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for neurological conditions affecting brain development. This specialized test focuses on identifying mutations in the TUBB2B gene, which plays a critical role in neuronal migration and cortical development during fetal brain formation.

What is TUBB2B Gene Polymicrogyria?

Polymicrogyria is a complex brain malformation characterized by excessive folding of the brain’s surface and abnormal cortical layering. The asymmetric form specifically affects one hemisphere more than the other, leading to varied neurological manifestations. The TUBB2B gene encodes beta-tubulin, a fundamental protein essential for microtubule formation and proper neuronal migration during embryonic development.

What Does This Test Detect?

Our advanced NGS-based genetic test specifically identifies:

  • Pathogenic variants in the TUBB2B gene associated with asymmetric polymicrogyria
  • Missense mutations affecting tubulin protein function
  • De novo and inherited genetic variations
  • Specific nucleotide changes impacting brain development pathways
  • Genetic markers for cortical malformation disorders

Who Should Consider This Test?

Clinical Indications and Symptoms

This genetic test is recommended for individuals presenting with:

  • Developmental delays and intellectual disability
  • Seizures or epilepsy of unknown origin
  • Motor impairments and movement disorders
  • Asymmetric brain findings on MRI scans
  • Family history of brain malformations or neurological conditions
  • Unexplained cerebral palsy-like symptoms
  • Congenital neurological abnormalities

Key Benefits of Genetic Testing

Undergoing the TUBB2B gene test provides numerous advantages:

  • Accurate Diagnosis: Confirms the genetic basis of neurological symptoms
  • Treatment Guidance: Helps tailor appropriate therapeutic interventions
  • Prognostic Information: Provides insight into disease progression and outcomes
  • Family Planning: Enables informed reproductive decisions
  • Early Intervention: Facilitates timely support and rehabilitation services
  • Research Contribution: Advances understanding of rare neurological disorders

Understanding Your Test Results

Interpretation Guidelines

Our comprehensive genetic report includes:

  • Positive Result: Indicates a pathogenic variant in the TUBB2B gene, confirming the genetic diagnosis of asymmetric polymicrogyria
  • Negative Result: Suggests no detectable mutation in the TUBB2B gene, though other genetic causes should be considered
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines inheritance patterns for family members

All results are accompanied by detailed genetic counseling to ensure proper understanding and appropriate next steps.

Test Details and Pricing

Test Component Details
Test Name TUBB2B Gene Polymicrogyria Asymmetric 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

Pre-Test Requirements

Before scheduling your test, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to create family pedigree chart
  • Discussion of testing implications with healthcare provider
  • Understanding of potential outcomes and their significance

Nationwide 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, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic counselors and healthcare professionals ensures accessible, high-quality care nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about neurological symptoms affect your quality of life. Our TUBB2B Gene Polymicrogyria Asymmetric NGS Genetic DNA Test provides the answers you need for informed medical decisions and comprehensive care planning.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our dedicated team is ready to guide you through every step of the testing process and help you understand your genetic health.

Early genetic diagnosis can make a significant difference in managing neurological conditions and improving long-term outcomes. Trust our expertise in pediatric genetics and dysmorphology to provide the comprehensive testing and support your family deserves.