DMD Mutation Screening 79 Exons Prenatal Test
Comprehensive Prenatal Genetic Screening for Duchenne Muscular Dystrophy
The DMD Mutation Screening 79 Exons Prenatal test represents a cutting-edge genetic diagnostic approach designed specifically for expectant parents concerned about the risk of Duchenne Muscular Dystrophy (DMD) in their developing baby. This comprehensive screening provides crucial insights during pregnancy, allowing families to make informed decisions and prepare for potential healthcare needs.
What Does This Test Measure and Detect?
This advanced prenatal screening utilizes Multiplex Ligation-dependent Probe Amplification (MLPA) technology to thoroughly examine all 79 exons of the dystrophin gene. The test specifically detects:
- Large-scale deletions in the DMD gene
- Gene duplications affecting dystrophin production
- Mutations responsible for Duchenne Muscular Dystrophy
- Genetic variations that disrupt normal muscle function
The dystrophin gene, located on the X chromosome, is essential for maintaining muscle cell integrity. Mutations in this gene lead to progressive muscle weakness and degeneration characteristic of DMD.
Who Should Consider This Prenatal Screening?
This test is particularly recommended for:
- Pregnant women with a family history of Duchenne Muscular Dystrophy
- Couples where the mother is a known carrier of DMD mutations
- Families with previous children affected by muscular dystrophy
- Women with elevated risk factors identified through carrier screening
- Expectant parents seeking comprehensive prenatal genetic information
Key Benefits of DMD Mutation Screening
Choosing this prenatal screening offers numerous advantages:
- Early Detection: Identify DMD mutations during pregnancy for timely intervention
- Informed Decision-Making: Provide families with crucial information for healthcare planning
- Comprehensive Analysis: Screen all 79 exons for complete genetic assessment
- Advanced Technology: Utilize MLPA methodology for accurate results
- Rapid Turnaround: Receive results within 7-10 days
- Professional Guidance: Access genetic counseling and medical support
Understanding Your Test Results
Your DMD Mutation Screening results will provide clear insights into your baby’s genetic status:
- Normal Result: No detectable DMD mutations found, indicating low risk for Duchenne Muscular Dystrophy
- Positive Result: Identified mutations in the dystrophin gene, requiring further genetic counseling
- Carrier Status: Important information for female fetuses regarding future reproductive decisions
- Variant of Unknown Significance: Rare genetic findings that may require additional testing
All positive results include comprehensive genetic counseling to help you understand the implications and available options.
Test Pricing and Availability
| Test Feature | Details |
|---|---|
| Test Name | DMD Mutation Screening 79 Exons Prenatal |
| Regular Price | $900 USD |
| Discount Price | $650 USD |
| Turnaround Time | 7-10 Days |
| Sample Type | Amniotic Fluid / Chorionic Villi / Cord Blood |
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, with convenient locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible prenatal genetic testing for families nationwide.
Book Your DMD Mutation Screening Today
Take the important step toward comprehensive prenatal genetic screening. Our experienced genetic counselors and medical professionals are ready to assist you through this process. Contact us today to schedule your DMD Mutation Screening 79 Exons Prenatal test.
Call or WhatsApp: +1(267) 388-9828
Secure your family’s health future with advanced prenatal genetic screening from General Genetics Corporation – your trusted partner in genetic diagnostics.
