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TUBB2B Gene Microcephaly NGS Genetic DNA Test

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

-29%

The TUBB2B Gene Microcephaly NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the TUBB2B gene, which plays a critical role in brain development and neuronal migration. This specialized test utilizes Next-Generation Sequencing (NGS) technology to detect pathogenic variants associated with congenital microcephaly, cortical malformations, and neurodevelopmental disorders. The test is particularly valuable for infants and children presenting with abnormally small head circumference, developmental delays, seizures, or neurological abnormalities. By providing precise genetic diagnosis, this test enables targeted medical management, informed family planning decisions, and personalized therapeutic interventions. Results are typically available within 3-4 weeks from sample collection. The test costs $500 USD and requires either blood sample, extracted DNA, or one drop of blood on an FTA card. Genetic counseling is recommended before testing to ensure proper interpretation and clinical correlation.

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TUBB2B Gene Microcephaly NGS Genetic DNA Test

Comprehensive Genetic Analysis for Brain Development Disorders

The TUBB2B Gene Microcephaly NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations responsible for congenital microcephaly and associated neurological conditions. This specialized test focuses on the TUBB2B gene, which encodes beta-tubulin, a crucial protein component of microtubules essential for proper neuronal migration and brain development during embryogenesis.

What Does This Test Measure?

This advanced genetic test specifically targets and analyzes the TUBB2B gene using Next-Generation Sequencing technology to detect:

  • Pathogenic mutations in the TUBB2B gene associated with microcephaly
  • Variants affecting tubulin structure and function
  • Genetic alterations disrupting neuronal migration patterns
  • Mutations linked to cortical malformations and brain development abnormalities
  • Inherited or de novo genetic changes affecting neurodevelopment

Who Should Consider This Test?

This genetic test is particularly recommended for individuals presenting with:

  • Congenital microcephaly (abnormally small head circumference at birth)
  • Developmental delays and intellectual disability
  • Seizures or epilepsy of unknown origin
  • Abnormal brain imaging findings showing cortical malformations
  • Family history of neurodevelopmental disorders
  • Unexplained neurological symptoms in infancy or childhood
  • Suspected tubulinopathy-related conditions

Clinical Benefits of TUBB2B Genetic Testing

Undergoing the TUBB2B Gene Microcephaly NGS Genetic DNA Test provides numerous clinical advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation of TUBB2B-related disorders
  • Personalized Treatment Planning: Enables targeted therapeutic interventions based on specific genetic findings
  • Family Planning Guidance: Offers valuable information for genetic counseling and reproductive decisions
  • Prognostic Information: Helps predict disease progression and potential complications
  • Early Intervention: Facilitates timely implementation of developmental support services
  • Research Contribution: Contributes to ongoing scientific understanding of neurogenetic disorders

Understanding Your Test Results

Your TUBB2B genetic test results will be carefully interpreted by our team of certified genetic counselors and medical geneticists:

  • Positive Result: Indicates the presence of a pathogenic mutation in the TUBB2B gene, confirming the genetic basis of observed symptoms
  • Negative Result: Suggests no disease-causing variants were detected in the TUBB2B gene, though other genetic causes should be considered
  • Variant of Uncertain Significance (VUS): Identifies genetic changes whose clinical significance requires further investigation
  • Carrier Status: Determines if an individual carries one copy of a mutated gene without showing symptoms

All results include comprehensive interpretation and recommendations for next steps in medical management.

Test Details and Pricing

Test Parameter Details
Test Name TUBB2B Gene Microcephaly NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood or Extracted DNA or One drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology
Specialty Pediatrics, Genetics
Disease Category Dysmorphology, Neurogenetics

Pre-Test Requirements

Before scheduling your TUBB2B genetic test, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session to discuss testing implications
  • Development of a detailed family pedigree chart
  • Review of previous neurological evaluations and imaging studies
  • Discussion of potential outcomes and their clinical significance

Nationwide Testing Availability

We proudly offer the TUBB2B Gene Microcephaly NGS Genetic DNA Test at our state-of-the-art facilities across the United States. Our network includes specialized testing centers in:

  • New York City, NY
  • Los Angeles, CA
  • Chicago, IL
  • Houston, TX
  • Phoenix, AZ
  • Philadelphia, PA
  • San Antonio, TX
  • San Diego, CA
  • Dallas, TX
  • San Jose, CA

And many other major metropolitan areas throughout the country.

Take the Next Step Toward Genetic Clarity

If you or your child are experiencing symptoms suggestive of TUBB2B-related disorders, don’t wait to seek answers. Our comprehensive genetic testing provides the clarity needed for informed medical decisions and personalized care planning.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and TUBB2B testing appointment. Our dedicated team of genetic specialists is ready to guide you through every step of the testing process and help you understand your results.

Early genetic diagnosis can make a significant difference in managing neurodevelopmental conditions and optimizing long-term outcomes. Contact us now to begin your journey toward genetic understanding and personalized medical care.

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