UPF3B Gene Mental Retardation X-Linked Type 14 NGS Genetic DNA Test
Comprehensive Genetic Testing for X-Linked Intellectual Disability
The UPF3B Gene Mental Retardation X-Linked Type 14 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for inherited intellectual disabilities. This advanced testing methodology provides families and healthcare providers with critical information for understanding the genetic basis of cognitive developmental disorders.
What Does This Test Measure?
This specialized genetic test specifically analyzes the UPF3B gene located on the X chromosome using Next Generation Sequencing (NGS) technology. The test detects:
- Point mutations and small insertions/deletions in the UPF3B gene
- Genetic variations associated with X-linked mental retardation type 14
- Pathogenic variants affecting nonsense-mediated mRNA decay pathways
- Inheritance patterns specific to X-linked disorders
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with:
- Unexplained intellectual disability or developmental delays
- Family history of X-linked mental retardation
- Multiple male family members affected by cognitive impairments
- Suspected genetic neurological disorders with unclear diagnosis
- Planning for family genetic counseling and risk assessment
Key Benefits of UPF3B Genetic Testing
- Accurate Diagnosis: Provides definitive identification of UPF3B gene mutations
- Family Planning Guidance: Enables informed reproductive decisions
- Early Intervention: Facilitates timely therapeutic interventions
- Genetic Counseling: Supports comprehensive family risk assessment
- Treatment Planning: Guides personalized management strategies
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 UPF3B mutation, confirming X-linked mental retardation type 14 diagnosis
- Negative Result: Suggests absence of detectable UPF3B mutations, though other genetic causes may need investigation
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Identifies individuals who carry the mutation but may not show symptoms
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
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, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality genetic testing services nationwide.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about genetic neurological conditions affect your family’s future. Our comprehensive UPF3B genetic testing provides the answers you need for informed healthcare decisions. Our team of genetic counselors and neurologists is ready to support you through every step of the testing process.
Call us today at +1(267) 388-9828 to schedule your appointment or book your test online. Take control of your genetic health with confidence and clarity.
