CD96 Gene C Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Developmental Disorders
The CD96 Gene C Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the CD96 gene, which are associated with C syndrome – a rare genetic disorder characterized by distinctive facial features, intellectual disability, and developmental delays. This advanced genetic test utilizes Next-Generation Sequencing (NGS) technology to provide comprehensive analysis of the CD96 gene, offering families and healthcare providers crucial diagnostic information for informed medical decision-making.
What Does the CD96 Gene C Syndrome Test Detect?
This specialized genetic test specifically targets and analyzes the CD96 gene for pathogenic variants that cause C syndrome. The test measures:
- Point mutations and small insertions/deletions in the CD96 gene
- Copy number variations affecting the CD96 gene region
- Specific genetic markers associated with developmental disorders
- Variant classification according to ACMG guidelines
Who Should Consider This Genetic Test?
This test is particularly recommended for individuals presenting with:
- Characteristic facial dysmorphic features including trigonocephaly
- Developmental delays and intellectual disability
- Growth abnormalities and skeletal anomalies
- Family history of similar developmental conditions
- Unexplained multiple congenital anomalies
- Suspected genetic syndromes with overlapping features
Key Benefits of CD96 Gene Testing
- Accurate Diagnosis: Provides definitive genetic confirmation of C syndrome
- Early Intervention: Enables timely therapeutic interventions and support services
- Family Planning: Offers valuable information for genetic counseling and reproductive decisions
- Personalized Care: Guides development of individualized treatment plans
- Prognostic Information: Helps predict disease progression and management needs
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our team of certified genetic counselors and medical geneticists. Results typically fall into three categories:
- Positive Result: Indicates the presence of a pathogenic CD96 gene mutation consistent with C syndrome diagnosis
- Negative Result: Suggests no detectable CD96 gene mutations, though other genetic causes may need investigation
- Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further evaluation
All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps.
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, with branches in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality genetic testing services nationwide.
Take the Next Step Toward Genetic Clarity
If you or your child are experiencing symptoms suggestive of C syndrome or related developmental disorders, the CD96 Gene C Syndrome NGS Genetic DNA Test can provide the answers you need. Our experienced genetic counselors are available to discuss your concerns and guide you through the testing process.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Take control of your genetic health journey with confidence and clarity.
