Alpha Thalassemia HBA1 HBA2 Deletion/Duplication Analysis Test
Comprehensive Genetic Testing for Hemoglobin Disorders
The Alpha Thalassemia HBA1 HBA2 Deletion/Duplication Analysis Test represents a cutting-edge approach to diagnosing inherited blood disorders that affect hemoglobin production. This specialized genetic test plays a crucial role in identifying alpha thalassemia, a condition characterized by reduced or absent synthesis of alpha-globin chains due to deletions or duplications in the HBA1 and HBA2 genes located on chromosome 16.
What This Advanced Test Detects
This comprehensive analysis specifically targets:
- Complete gene deletions affecting HBA1 and HBA2
- Partial gene deletions impacting alpha-globin production
- Gene duplications that may affect hemoglobin synthesis
- Various combinations of deletion patterns
- Silent carrier states and trait conditions
Who Should Consider This Genetic Analysis?
Clinical Indications and Symptoms
This test is recommended for individuals experiencing:
- Unexplained microcytic hypochromic anemia
- Family history of thalassemia or hemoglobin disorders
- Ethnic backgrounds with higher thalassemia prevalence (Southeast Asian, Mediterranean, African, Middle Eastern)
- Abnormal hemoglobin electrophoresis results
- Couples planning pregnancy with known thalassemia risk factors
- Newborns with hemoglobin Bart’s or hydrops fetalis
Significant Benefits of Genetic Testing
Comprehensive Diagnostic Advantages
- Accurate Diagnosis: Provides definitive identification of alpha thalassemia mutations
- Family Planning Guidance: Enables informed reproductive decisions and genetic counseling
- Early Intervention: Facilitates timely management of potential complications
- Personalized Treatment: Guides appropriate therapeutic approaches based on genetic profile
- Carrier Detection: Identifies silent carriers who may pass mutations to offspring
Understanding Your Test Results
Interpretation Guidance
Your genetic test results will be carefully analyzed and explained by our expert genetic counselors:
- Normal Results: No deletions or duplications detected in HBA1/HBA2 genes
- Silent Carrier: Single gene deletion – typically asymptomatic
- Alpha Thalassemia Trait: Two gene deletions – mild anemia possible
- Hemoglobin H Disease: Three gene deletions – moderate to severe anemia
- Hydrops Fetalis: Four gene deletions – severe, often fatal condition
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $340 |
| Regular Price | $450 |
Nationwide Accessibility
We have conveniently located branches across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, and many other cities. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.
Take Control of Your Genetic Health Today
Don’t wait to get the answers you need about potential hemoglobin disorders. Our expert team of genetic specialists and hematologists are ready to provide comprehensive testing and personalized guidance. Schedule your Alpha Thalassemia HBA1 HBA2 Deletion/Duplication Analysis Test today and take the first step toward understanding your genetic health.
Call or WhatsApp us now at +1(267) 388-9828 to book your appointment or get more information about this essential genetic screening.
With results typically available within 2-3 weeks and our special discounted price of $340, there’s no better time to invest in your genetic health and peace of mind.
