IL11RA Gene Craniosynostosis and Dental Anomalies NGS Genetic DNA Test
Comprehensive Genetic Testing for Craniofacial Disorders
The IL11RA Gene Craniosynostosis and Dental Anomalies NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for patients presenting with complex craniofacial abnormalities. This advanced genetic analysis specifically targets the IL11RA (Interleukin 11 Receptor Alpha) gene, which plays a crucial role in bone development and cranial suture formation. When mutations occur in this gene, they can lead to premature fusion of skull bones (craniosynostosis) and various dental anomalies, creating significant clinical challenges that require precise diagnosis and specialized management.
What This Test Measures and Detects
Our state-of-the-art Next-Generation Sequencing (NGS) technology comprehensively analyzes the entire IL11RA gene to identify:
- Pathogenic variants and mutations in the IL11RA gene
- Single nucleotide polymorphisms (SNPs) associated with craniosynostosis
- Insertions, deletions, and copy number variations
- Novel genetic variants that may impact protein function
- Specific mutations linked to dental development abnormalities
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for individuals presenting with:
- Infants and children with premature cranial suture fusion
- Patients with abnormal head shape or skull deformities
- Individuals with delayed or abnormal dental development
- Patients with family history of craniosynostosis disorders
- Children experiencing dental anomalies alongside cranial abnormalities
- Patients with suspected IL11RA-related genetic syndromes
Key Benefits of IL11RA Genetic Testing
- Accurate Diagnosis: Provides definitive molecular confirmation of IL11RA-related disorders
- Treatment Guidance: Informs surgical planning and timing for craniosynostosis correction
- Family Planning: Enables genetic counseling and recurrence risk assessment
- Early Intervention: Facilitates timely management of dental and cranial abnormalities
- Comprehensive Care: Supports multidisciplinary approach involving genetics, neurosurgery, and dentistry
Understanding Your Test Results
Our comprehensive genetic report provides clear interpretation of your results:
- Positive Result: Identifies a pathogenic variant in the IL11RA gene, confirming the genetic basis of symptoms
- Negative Result: No disease-causing variants detected, though clinical evaluation remains important
- Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
- Carrier Status: Determines if individuals carry mutations that could affect future generations
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
GGC DNA maintains testing facilities across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and medical professionals ensures accessible, high-quality genetic testing services nationwide.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about craniosynostosis and dental anomalies delay proper diagnosis and treatment. Our IL11RA genetic testing provides the answers you need for informed medical decisions and comprehensive care planning. Contact our genetic specialists today to schedule your test and begin your journey toward genetic clarity.
Call or WhatsApp: +1(267) 388-9828 to book your IL11RA Gene Craniosynostosis and Dental Anomalies NGS Genetic DNA Test today!
