Thalassemia Beta Trio Prenatal Mutation Detection Test
Comprehensive Genetic Screening for Beta-Thalassemia
The Thalassemia Beta Trio Prenatal Mutation Detection Test represents a significant advancement in prenatal genetic screening, offering comprehensive analysis of beta-thalassemia mutations in both prospective parents and the developing fetus. This sophisticated molecular diagnostic procedure provides crucial information that enables healthcare providers and families to make informed decisions about pregnancy management and future family planning.
What This Test Measures and Detects
This comprehensive genetic screening test specifically targets and analyzes:
- Over 100 distinct mutations in the HBB gene responsible for beta-thalassemia
- Carrier status in both biological parents
- Fetal genetic status for beta-thalassemia mutations
- Risk assessment for homozygous or compound heterozygous conditions
- Inheritance patterns within the family genetic profile
Who Should Consider This Test
This prenatal genetic screening is particularly recommended for:
- Couples with family history of thalassemia or hemoglobinopathies
- Individuals from ethnic backgrounds with high thalassemia prevalence (Mediterranean, Middle Eastern, South Asian, African)
- Couples where one partner has been identified as a beta-thalassemia carrier
- Pregnant women with abnormal hemoglobin electrophoresis results
- Families seeking comprehensive prenatal genetic information
- Couples undergoing advanced maternal age pregnancies
Key Benefits of Thalassemia Beta Trio Testing
- Early Risk Assessment: Provides early detection of genetic risks before birth
- Informed Decision Making: Enables families to make educated choices about pregnancy management
- Comprehensive Family Planning: Offers valuable information for future family planning decisions
- Medical Preparedness: Allows healthcare teams to prepare for potential specialized care needs
- Psychological Preparation: Helps families emotionally prepare for various outcomes
- Advanced Technology: Utilizes cutting-edge PCR and sequencing methodologies
Understanding Your Test Results
Your test results will provide detailed genetic information about:
- Parental Carrier Status: Identifies whether each parent carries beta-thalassemia mutations
- Fetal Genetic Status: Determines if the fetus has inherited thalassemia mutations
- Inheritance Pattern Analysis: Shows how genetic traits are being passed to the fetus
- Risk Assessment: Calculates the probability of the child developing thalassemia
Our genetic counselors will help you understand your results and discuss next steps based on the findings.
Test Pricing Information
| Test Description | Price (USD) |
|---|---|
| Discount Price | $526 |
| Regular Price | $586 |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified laboratories ensures consistent, high-quality testing standards nationwide.
Sample Requirements and Processing
Sample Collection:
- 4 mL (2 mL minimum) whole blood in 1 Lavender top (EDTA) tube from both parents
- 10 mL (5 mL minimum) Amniotic fluid in sterile screw-capped container
- Ship refrigerated – DO NOT FREEZE samples
Required Documentation:
- Duly filled Prenatal Genetic testing consent form (Form 18)
- Genomics Clinical information requisition form (Form 20)
Turnaround Time: Sample received by Monday 11 AM; Report delivered Friday
Take the Next Step Toward Genetic Clarity
Don’t leave your family’s genetic health to chance. Our Thalassemia Beta Trio Prenatal Mutation Detection Test provides the comprehensive information you need for informed family planning and pregnancy management. With over 100 mutations analyzed using advanced PCR and sequencing technology, you can trust our expertise in genetic diagnostics.
Call us today at +1(267) 388-9828 to schedule your comprehensive genetic screening or to speak with our genetic counseling team. Take control of your family’s genetic health with confidence and clarity.
