MSX2 Gene Craniosynostosis Type 2 NGS Genetic DNA Test
Comprehensive Genetic Testing for Craniosynostosis
The MSX2 Gene Craniosynostosis Type 2 NGS Genetic DNA Test represents a breakthrough in pediatric genetic diagnostics, offering families and healthcare providers precise molecular insights into craniosynostosis type 2. This advanced genetic test utilizes next-generation sequencing technology to analyze the MSX2 gene, which plays a critical role in skull development and suture formation during fetal growth.
What Does This Test Measure?
This sophisticated genetic analysis specifically targets and sequences the MSX2 gene to identify pathogenic variants associated with craniosynostosis type 2. The test detects:
- Point mutations in the MSX2 gene coding regions
- Small insertions and deletions affecting gene function
- Regulatory region variations impacting gene expression
- Known pathogenic variants linked to premature suture fusion
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with:
- Infants with abnormal head shape or premature fontanelle closure
- Children showing signs of craniofacial dysmorphism
- Patients with family history of craniosynostosis
- Individuals with suspected Boston-type craniosynostosis
- Patients undergoing evaluation for cranial surgery planning
- Families seeking genetic counseling for recurrence risk assessment
Key Benefits of MSX2 Genetic Testing
- Early Diagnosis: Enables prompt intervention before complications develop
- Surgical Planning: Provides crucial information for cranial reconstruction procedures
- Family Counseling: Helps assess recurrence risks for future pregnancies
- Personalized Care: Guides individualized treatment approaches
- Peace of Mind: Offers definitive answers for concerned families
Understanding Your Test Results
Our comprehensive genetic report provides clear interpretation of your results:
- Positive Result: Indicates a pathogenic MSX2 mutation is present, confirming craniosynostosis type 2 diagnosis
- Negative Result: Suggests no MSX2 mutation detected, though other genetic causes may need investigation
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Important information for family planning decisions
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | MSX2 Gene Craniosynostosis Type 2 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) |
Pre-Test Requirements
Before scheduling your test, please ensure:
- Complete clinical history of the patient
- Genetic counseling session to create family pedigree chart
- Documentation of affected family members with craniosynostosis
- Referral from pediatrician or genetic specialist
Nationwide Testing Availability
We have testing facilities 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 network of certified genetic counselors and pediatric specialists ensures comprehensive care throughout your testing journey.
Take the Next Step Toward Answers
Don’t let uncertainty about craniosynostosis type 2 affect your family’s peace of mind. Our advanced MSX2 genetic testing provides the clarity you need for informed medical decisions and proper treatment planning. With our discounted price of $500 USD and comprehensive genetic analysis, you’re investing in your child’s health and future.
Ready to schedule your test? Call our genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and guide you through the testing process with compassion and expertise.
