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FOXP2 Gene Speech-Language Disorder Type 1 NGS Genetic DNA Test

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

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The FOXP2 Gene Speech-Language Disorder Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the FOXP2 gene, which is crucial for speech and language development. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variants associated with childhood apraxia of speech and other language disorders. The test is particularly valuable for children experiencing significant speech delays, articulation difficulties, and language comprehension challenges. By identifying the underlying genetic cause, healthcare providers can develop targeted intervention strategies and provide families with accurate prognosis information. The test costs $500 USD and offers reliable results within 3-4 weeks, helping families understand the genetic basis of speech-language disorders and guiding appropriate therapeutic approaches.

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FOXP2 Gene Speech-Language Disorder Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Speech and Language Disorders

The FOXP2 Gene Speech-Language Disorder Type 1 NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for speech and language impairments. This advanced genetic test specifically targets the FOXP2 gene, which plays a fundamental role in the development of neural circuits essential for speech production and language comprehension. Discovered as the first gene directly linked to speech and language development, FOXP2 mutations can cause significant communication challenges that often manifest in early childhood.

What Does This Test Measure?

This comprehensive NGS-based genetic test analyzes the entire FOXP2 gene sequence to identify pathogenic variants, including:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions (indels)
  • Copy number variations affecting the FOXP2 gene
  • Regulatory region abnormalities
  • Novel genetic variants with potential clinical significance

The test utilizes state-of-the-art Next-Generation Sequencing technology, providing unparalleled accuracy and comprehensive coverage of the FOXP2 gene region. This advanced methodology ensures detection of even rare genetic variants that might be missed by conventional testing methods.

Who Should Consider This Test?

This genetic test is particularly recommended for individuals presenting with:

  • Severe childhood apraxia of speech (CAS)
  • Significant speech delay beyond typical developmental milestones
  • Articulation difficulties that persist despite speech therapy
  • Language comprehension challenges
  • Family history of speech and language disorders
  • Oral motor coordination difficulties
  • Grammatical processing impairments
  • Developmental verbal dyspraxia

Clinical Benefits of FOXP2 Genetic Testing

Undergoing FOXP2 genetic testing provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out FOXP2-related speech disorders
  • Personalized Treatment: Guides targeted speech therapy interventions
  • Prognostic Information: Helps predict long-term outcomes and progression
  • Family Planning: Provides recurrence risk information for future pregnancies
  • Early Intervention: Enables timely therapeutic approaches
  • Educational Planning: Supports appropriate school accommodations
  • Genetic Counseling: Facilitates comprehensive family management

Understanding Your Test Results

Your FOXP2 genetic test results will fall into one of several categories:

  • Positive Result: Indicates a pathogenic variant in the FOXP2 gene is present, confirming the genetic basis of speech-language disorder
  • Negative Result: Suggests no FOXP2 mutation was detected, though other genetic or environmental factors may contribute to symptoms
  • Variant of Uncertain Significance (VUS): Identifies a genetic change whose clinical significance is currently unknown
  • Carrier Status: May identify individuals who carry the mutation but may not exhibit symptoms

All results are accompanied by detailed interpretation from our board-certified genetic counselors and clinical geneticists, ensuring you receive comprehensive guidance for next steps.

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Nationwide Testing Availability

We proudly offer FOXP2 genetic testing services across the United States, with convenient 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 collection centers ensures accessible testing for families nationwide.

Pre-Test Requirements

Before scheduling your FOXP2 genetic test, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to discuss testing implications
  • Family pedigree chart development
  • Informed consent process completion
  • Insurance pre-authorization if applicable

Take the Next Step Toward Understanding

If you or your child is experiencing speech and language challenges, the FOXP2 Gene Speech-Language Disorder Type 1 NGS Genetic DNA Test can provide the answers you need. Our team of genetic specialists is ready to guide you through the testing process and help interpret your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your FOXP2 genetic test. Take control of your genetic health journey with confidence and clarity.