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CTNNB1 Gene Mental Retardation Autosomal Dominant Type 19 Genetic Test

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

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The CTNNB1 Gene Mental Retardation Autosomal Dominant Type 19 NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the CTNNB1 gene, which plays a crucial role in brain development and function. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations associated with autosomal dominant mental retardation type 19. The test is particularly valuable for individuals experiencing developmental delays, intellectual disabilities, or neurological symptoms that may have a genetic basis. By providing precise genetic information, this test enables accurate diagnosis, informed family planning decisions, and personalized management strategies. The test is available for $500 USD and provides results within 3-4 weeks, offering families and healthcare providers critical insights into neurodevelopmental conditions.

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CTNNB1 Gene Mental Retardation Autosomal Dominant Type 19 NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurodevelopmental Disorders

The CTNNB1 Gene Mental Retardation Autosomal Dominant Type 19 NGS Genetic DNA Test represents a significant advancement in neurological genetic diagnostics. This specialized test focuses on identifying mutations in the CTNNB1 gene, which encodes beta-catenin—a critical protein involved in neuronal development, synaptic function, and brain architecture. Understanding these genetic variations provides essential insights into the underlying causes of neurodevelopmental disorders and enables targeted intervention strategies.

What This Test Measures and Detects

Our advanced NGS-based genetic analysis specifically targets:

  • Pathogenic variants in the CTNNB1 gene associated with autosomal dominant mental retardation type 19
  • Single nucleotide variants (SNVs) and small insertions/deletions (indels)
  • Copy number variations affecting the CTNNB1 gene region
  • Genetic markers linked to impaired Wnt signaling pathway function
  • Variants affecting beta-catenin protein structure and function

Who Should Consider This Genetic Test

This comprehensive genetic evaluation is recommended for individuals presenting with:

  • Unexplained developmental delays in childhood
  • Intellectual disability of unknown origin
  • Family history of neurodevelopmental disorders
  • Speech and language development concerns
  • Motor coordination difficulties
  • Behavioral abnormalities without clear cause
  • Suspected genetic basis for neurological symptoms

Key Benefits of CTNNB1 Genetic Testing

Undergoing this specialized genetic analysis offers numerous advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation of CTNNB1-related disorders
  • Family Planning Guidance: Enables informed reproductive decisions for at-risk families
  • Personalized Management: Facilitates tailored intervention and therapy approaches
  • Prognostic Information: Helps predict disease progression and potential complications
  • Research Contribution: Advances understanding of neurodevelopmental genetics
  • Early Intervention: Supports timely implementation of appropriate therapies

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret your results:

  • Positive Result: Indicates the presence of a pathogenic CTNNB1 variant, confirming the genetic diagnosis
  • Negative Result: Suggests that CTNNB1 mutations are not the cause of symptoms, guiding further diagnostic evaluation
  • Variant of Uncertain Significance: Identifies genetic changes requiring additional research and family studies
  • Carrier Status: Provides information about inheritance patterns and recurrence risks

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

Pre-Test Requirements

To ensure optimal testing outcomes, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session with our specialists
  • Development of detailed family pedigree chart
  • Discussion of testing implications and potential outcomes

Nationwide Testing Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas 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 neurological specialists ensures comprehensive support throughout your testing journey.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about neurological symptoms affect your quality of life. Our CTNNB1 Gene Mental Retardation Autosomal Dominant Type 19 NGS Genetic DNA Test provides the answers you need for informed healthcare decisions. Contact our genetic specialists today to schedule your consultation and testing appointment.

Call or WhatsApp: +1(267) 388-9828
Book Your Test Today and Receive Professional Genetic Counseling

Our team of neurological genetics experts is ready to guide you through the testing process, interpret your results, and provide personalized recommendations based on your genetic profile. Take control of your neurological health with advanced genetic insights from America’s leading genetics corporation.

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