ZDHHC17 Gene Huntington Disease NGS Genetic DNA Test
Comprehensive Genetic Testing for Huntington Disease Risk Assessment
The ZDHHC17 Gene Huntington Disease NGS Genetic DNA Test represents a significant advancement in neurological genetic testing, providing crucial insights into an individual’s genetic predisposition to Huntington disease. This sophisticated diagnostic tool utilizes state-of-the-art Next-Generation Sequencing technology to analyze the ZDHHC17 gene, which plays a critical role in neurological function and has been linked to Huntington disease pathogenesis.
What Does This Test Measure?
This comprehensive genetic test specifically targets and sequences the ZDHHC17 gene, identifying:
- Pathogenic mutations associated with Huntington disease
- Genetic variations that may increase disease susceptibility
- Specific nucleotide changes affecting protein function
- Inheritance patterns relevant to neurological disorders
Who Should Consider This Test?
This genetic test is particularly recommended for individuals experiencing:
- Family history of Huntington disease or related neurological conditions
- Early neurological symptoms including movement disorders
- Cognitive changes or behavioral symptoms with unknown causes
- Unexplained progressive neurological deterioration
- Planning for family and reproductive decisions
Key Benefits of ZDHHC17 Genetic Testing
- Early Risk Assessment: Identify genetic predisposition before symptom onset
- Personalized Healthcare: Enable targeted monitoring and preventive strategies
- Family Planning: Make informed decisions about reproductive choices
- Treatment Guidance: Support neurologists in developing appropriate care plans
- Peace of Mind: Provide clarity about genetic status and future health risks
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our expert genetic counselors and neurologists:
- Positive Result: Indicates the presence of a pathogenic mutation, requiring comprehensive neurological evaluation and management planning
- Negative Result: Suggests absence of known disease-causing mutations in the ZDHHC17 gene
- Variant of Uncertain Significance: Identifies genetic changes requiring further research and monitoring
- Carrier Status: Determines if you carry genetic variations that could affect future generations
Test Details and Pricing
| Test Feature | Details |
|---|---|
| Test Name | ZDHHC17 Gene Huntington Disease 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 undergoing testing, we recommend:
- Comprehensive clinical history documentation
- Genetic counseling session with our specialists
- Development of detailed family pedigree chart
- Discussion of potential implications and psychological preparation
Nationwide 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, and San Jose. Our network of certified genetic counselors and neurological specialists ensures you receive comprehensive support throughout your testing journey.
Take Control of Your Neurological Health Today
Don’t wait to gain valuable insights into your genetic health. Our ZDHHC17 Gene Huntington Disease NGS Genetic DNA Test provides the clarity and information you need to make informed healthcare decisions. With our discounted price of $500 USD, advanced genetic testing is more accessible than ever.
Call us now at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our expert team is ready to guide you through every step of the process and answer any questions you may have about neurological genetic testing.
