HCFC1 Gene Mental Retardation X-Linked Type 3 NGS Genetic DNA Test
Comprehensive Genetic Testing for X-Linked Intellectual Disability
The HCFC1 Gene Mental Retardation X-Linked Type 3 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering families crucial insights into inherited intellectual disability conditions. This advanced testing methodology provides accurate detection of mutations in the HCFC1 gene, which plays a critical role in cognitive development and neurological function.
What Does This Test Measure?
Our comprehensive NGS-based test specifically targets the HCFC1 gene located on the X chromosome, analyzing it for pathogenic variants that cause X-linked mental retardation type 3. The test examines:
- Complete gene sequencing of HCFC1 using Next-Generation Sequencing technology
- Detection of point mutations, insertions, and deletions
- Identification of splice site variants affecting gene function
- Analysis of regulatory regions influencing gene expression
Who Should Consider This Test?
This genetic test is particularly important for individuals and families experiencing:
- Unexplained intellectual disability or developmental delays
- Family history of X-linked inheritance patterns of cognitive impairment
- Males with intellectual disability without clear diagnosis
- Families planning pregnancy with history of neurological disorders
- Individuals with co-occurring neurological symptoms
Key Benefits of HCFC1 Genetic Testing
- Accurate Diagnosis: Provides definitive identification of HCFC1 gene mutations with 99.9% accuracy
- Family Planning Guidance: Enables informed reproductive decisions and genetic counseling
- Early Intervention: Facilitates timely therapeutic interventions and support services
- Personalized Care: Helps tailor educational and therapeutic approaches to individual needs
- Clarification of Inheritance Patterns: Explains family history and recurrence risks
Understanding Your Test Results
Our comprehensive genetic counseling service helps you interpret your results:
- Positive Result: Indicates presence of pathogenic HCFC1 mutation; our genetic counselors provide detailed explanation of implications and management strategies
- Negative Result: Suggests absence of tested mutations; however, other genetic causes may still be present
- Variant of Uncertain Significance: Requires additional family studies and follow-up testing
- Carrier Status: Important information for female relatives regarding transmission risks
Test Details and Pricing
| Test Feature | Details |
|---|---|
| Test Name | HCFC1 Gene Mental Retardation X-Linked Type 3 NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 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
We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network ensures that quality genetic testing is accessible to families throughout the country.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your family’s future. Our team of genetic specialists and neurologists is ready to provide the comprehensive testing and counseling you need. Schedule your appointment today and take control of your genetic health.
Call us now at +1(267) 388-9828 to book your HCFC1 genetic test or schedule a genetic counseling session. Our compassionate team is available to answer your questions and guide you through the testing process.
