Beta Thalassemia HBB Full Gene Analysis Couple
Comprehensive Genetic Screening for Beta Thalassemia
Beta Thalassemia HBB Full Gene Analysis Couple represents a cutting-edge genetic diagnostic approach designed to identify mutations in the HBB gene responsible for Beta Thalassemia. This comprehensive screening provides couples with essential information about their genetic status, enabling informed family planning decisions and proactive healthcare management.
What This Test Measures and Detects
This advanced genetic analysis specifically targets the HBB gene located on chromosome 11, which encodes the beta-globin subunit of hemoglobin. The test utilizes Sanger sequencing technology to examine the entire coding region, splice sites, and promoter regions of the HBB gene. It identifies various mutation types including:
- Point mutations affecting beta-globin production
- Small insertions and deletions within the gene
- Splice site mutations impacting RNA processing
- Promoter region variations affecting gene expression
Who Should Consider This Genetic Screening
This comprehensive genetic analysis is particularly recommended for:
- Couples planning pregnancy with family history of thalassemia
- Individuals with Mediterranean, African, Middle Eastern, or Southeast Asian ancestry
- Partners experiencing unexplained anemia or abnormal blood counts
- Couples seeking pre-conception genetic counseling
- Individuals with known family members carrying thalassemia traits
Clinical Benefits of Genetic Testing
Undergoing Beta Thalassemia HBB Full Gene Analysis provides numerous advantages:
- Accurate assessment of genetic carrier status for both partners
- Early identification of potential risks for offspring
- Informed family planning decisions based on genetic information
- Access to appropriate genetic counseling and medical guidance
- Peace of mind through comprehensive genetic screening
Understanding Your Test Results
Your genetic analysis results will provide detailed information about your HBB gene status:
- Normal Results: No mutations detected in the HBB gene
- Carrier Status: Identification of one mutated HBB gene copy
- Affected Status: Detection of mutations in both HBB gene copies
- Variant of Unknown Significance: Rare genetic variations requiring further evaluation
All results are accompanied by comprehensive interpretation from our genetic specialists, ensuring you receive clear explanations and appropriate next-step recommendations.
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $376 |
| Regular Price | $500 |
Nationwide Testing Availability
We maintain comprehensive testing facilities across major metropolitan areas throughout the United States, 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 analysis with rapid turnaround times of 8-10 days.
Schedule Your Genetic Screening Today
Take the first step toward informed family planning and comprehensive genetic health assessment. Our experienced genetic counselors and medical professionals are ready to assist you with this important screening process.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your Beta Thalassemia HBB Full Gene Analysis Couple test and receive professional genetic counseling services.
