MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test
Understanding MSX2 Gene Parietal Foramina Type 1
Parietal foramina type 1 is a rare congenital condition characterized by symmetrical, oval-shaped defects in the parietal bones of the skull. These openings typically occur near the vertex of the skull and can vary in size from small, barely noticeable depressions to larger defects that may require medical intervention. The condition is inherited in an autosomal dominant pattern, meaning only one copy of the mutated gene is sufficient to cause the disorder.
What This Test Measures
The MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test utilizes advanced next-generation sequencing technology to comprehensively analyze the MSX2 gene for pathogenic mutations. This test specifically targets:
- Complete sequencing of the MSX2 gene coding regions
- Detection of point mutations, insertions, and deletions
- Identification of known pathogenic variants associated with parietal foramina
- Analysis of regulatory regions that may affect gene expression
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with specific clinical indications:
- Children or adults with symmetrical skull defects in the parietal region
- Individuals with family history of cranial abnormalities or parietal foramina
- Patients with unexplained developmental delays accompanied by skull anomalies
- Couples planning pregnancy with known family history of MSX2-related disorders
- Individuals with suspected genetic syndromes involving cranial development
Clinical Symptoms and Indications
- Visible or palpable skull defects in the parietal region
- Family history of craniofacial abnormalities
- Associated neurological symptoms in some cases
- Developmental concerns with cranial involvement
- Genetic counseling requirements for family planning
Benefits of MSX2 Genetic Testing
Undergoing the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test provides numerous clinical advantages:
- Accurate Diagnosis: Confirms or rules out MSX2-related parietal foramina with high precision
- Family Planning Guidance: Enables informed reproductive decisions for at-risk families
- Medical Management: Guides appropriate monitoring and intervention strategies
- Surgical Planning: Provides genetic information crucial for cranial surgical procedures
- Genetic Counseling: Supports comprehensive genetic counseling for affected families
- Early Intervention: Facilitates timely medical care and monitoring when needed
Understanding Your Test Results
Your MSX2 genetic test results will be carefully interpreted by our team of genetic specialists:
Positive Result
A positive result indicates the presence of a pathogenic mutation in the MSX2 gene. This confirms the diagnosis of parietal foramina type 1 and provides important information for:
- Medical management and monitoring recommendations
- Family member testing considerations
- Reproductive planning options
- Appropriate specialist referrals
Negative Result
A negative result suggests that no pathogenic MSX2 mutations were detected. However, this does not completely rule out the possibility of parietal foramina, as other genetic or environmental factors may be involved. Further evaluation may be recommended.
Variant of Uncertain Significance
In some cases, genetic changes of unknown clinical significance may be identified. These variants require careful interpretation and may necessitate additional family studies or follow-up testing.
Test Information and Pricing
| Test Component | Details |
|---|---|
| Test Name | MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood or Extracted DNA or One drop Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) Technology |
| Specialty | Pediatrics, Genetics |
| Disease Category | Dysmorphology |
Pre-Test Requirements
Before undergoing the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test, patients should provide:
- Complete clinical history of the patient
- Genetic counseling session to create a detailed family pedigree
- Documentation of affected family members with similar conditions
- Relevant medical imaging studies when available
Nationwide Testing Availability
We proudly offer the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test at our state-of-the-art facilities across the United States. Our comprehensive network includes testing centers in:
- New York City and surrounding areas
- Los Angeles and Southern California
- Chicago and the Midwest region
- Houston and Texas locations
- Phoenix and Arizona facilities
- All other major metropolitan areas nationwide
Take the Next Step Toward Genetic Clarity
If you or your family members are experiencing symptoms suggestive of parietal foramina or have concerns about inherited cranial conditions, the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test provides the answers you need. Our experienced genetic counselors and medical specialists are available to guide you through the testing process and help interpret your results.
Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your MSX2 genetic test. Take control of your genetic health with comprehensive, accurate testing from America’s leading genetics laboratory.
