DYNC1H1 Gene Mental Retardation Test USA - $500 | NGS Genetic Testing for Autosomal Dominant Type 13 | GGC DNA
TANC2 Gene Brain Disorders NGS Genetic DNA Test USA $500 | Comprehensive Neurodevelopmental Testing TANC2 Gene Brain Disorders NGS Genetic DNA Test Original price was: $700.Current price is: $500.
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DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 NGS Genetic DNA Test

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

-29%

The DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the DYNC1H1 gene responsible for autosomal dominant intellectual disability. This comprehensive test utilizes next-generation sequencing technology to detect specific genetic variations that cause developmental delays, cognitive impairment, and neurological symptoms. Individuals with family history of intellectual disability, developmental delays, or unexplained neurological symptoms should consider this test. The test provides crucial information for accurate diagnosis, personalized treatment planning, and informed family decisions. Results are typically available within 3-4 weeks from blood, extracted DNA, or blood spot samples. The test is priced at $500 USD with genetic counseling included to help interpret results and understand inheritance patterns.

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DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 NGS Genetic DNA Test

Comprehensive Genetic Testing for Intellectual Disability

The DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 NGS Genetic DNA Test represents a breakthrough in neurogenetic diagnostics, offering precise identification of mutations in the DYNC1H1 gene that cause autosomal dominant intellectual disability. This sophisticated testing approach provides families and healthcare providers with definitive answers about the genetic basis of developmental and cognitive challenges.

What This Advanced Genetic Test Detects

Our specialized NGS genetic test specifically targets the DYNC1H1 gene, which encodes the cytoplasmic dynein 1 heavy chain 1 protein. This crucial protein plays a fundamental role in intracellular transport within neurons, particularly in the movement of essential cellular components along microtubules. When mutations occur in this gene, they disrupt normal neuronal function and development, leading to the characteristic features of autosomal dominant mental retardation type 13.

  • Identifies pathogenic variants in the DYNC1H1 gene
  • Detects both inherited and de novo mutations
  • Analyzes the complete coding region for comprehensive coverage
  • Provides information about variant classification and clinical significance

Who Should Consider DYNC1H1 Genetic Testing?

This specialized genetic test is particularly valuable for individuals and families experiencing:

  • Unexplained intellectual disability or developmental delays
  • Family history of autosomal dominant inheritance patterns of cognitive impairment
  • Children with delayed motor milestones and speech development
  • Individuals with neurological symptoms including muscle weakness or coordination difficulties
  • Families seeking genetic counseling for family planning decisions
  • Patients with suspected neurodevelopmental disorders of unknown etiology

Significant Benefits of DYNC1H1 Genetic Testing

Choosing to undergo DYNC1H1 genetic testing provides numerous advantages for patients and families:

  • Accurate Diagnosis: Provides definitive answers about the genetic cause of intellectual disability
  • Personalized Care Planning: Enables targeted interventions and appropriate educational support
  • Family Risk Assessment: Identifies inheritance patterns and recurrence risks for family members
  • Early Intervention: Facilitates timely access to specialized therapies and support services
  • Genetic Counseling: Offers comprehensive guidance for future family planning decisions
  • Research Contribution: Contributes to ongoing scientific understanding of neurogenetic disorders

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your DYNC1H1 test results with clarity and compassion:

  • Positive Result: Indicates the presence of a pathogenic DYNC1H1 mutation, confirming the genetic diagnosis
  • Negative Result: Suggests that DYNC1H1 mutations are not the cause of symptoms, guiding further diagnostic evaluation
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical impact requires further investigation
  • Carrier Status: Provides information about inheritance risks for future generations

All results are accompanied by detailed explanations and recommendations from our certified genetic counselors, ensuring you have the support needed to make informed healthcare decisions.

Test Details and Pricing

Test Component Details
Test Name DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 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

Nationwide Accessibility and Support

GGC DNA maintains comprehensive testing facilities 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, and San Jose. Our network ensures that high-quality genetic testing is accessible to patients nationwide.

Our dedicated team of genetic specialists, including board-certified genetic counselors and molecular geneticists, provides personalized support throughout the testing process. We understand the emotional significance of genetic testing and are committed to delivering compassionate, confidential care.

Take the Next Step Toward Genetic Clarity

If you or a family member are experiencing symptoms suggestive of DYNC1H1-related intellectual disability, don’t wait to seek answers. Our comprehensive genetic testing provides the clarity needed to make informed healthcare decisions and access appropriate support services.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book the DYNC1H1 Gene Mental Retardation Autosomal Dominant Type 13 NGS Genetic DNA Test. Our genetic specialists are ready to guide you through every step of the testing process and help you understand your results with compassion and expertise.

Early genetic diagnosis can make a significant difference in managing neurodevelopmental conditions and planning for the future. Contact us now to begin your journey toward genetic understanding and personalized care.

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