Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test
The Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test is a cutting-edge genetic test that plays a crucial role in diagnosing Duchenne and Becker muscular dystrophy (DMD/BMD), conditions that primarily affect muscle strength and function. Understanding these genetic disorders is vital for early intervention and management, making this test an essential tool for neurologists and patients alike.
What Does the Test Measure?
This test specifically detects mutations in the dystrophin gene, which are responsible for DMD and BMD. By identifying these mutations, healthcare providers can better understand the genetic basis of muscle weakness in affected individuals.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Progressive muscle weakness
- Difficulty in walking or running
- Frequent falls
- Muscle cramps or stiffness
Additionally, those with a family history of muscular dystrophy should consider this test to assess their risk and take proactive steps towards management.
Benefits of Taking the Test
- Early diagnosis can lead to timely intervention and treatment.
- Helps in understanding the genetic nature of the disorder.
- Provides valuable information for family planning.
- Guides treatment decisions and management strategies.
Understanding Your Results
Results from the Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test will indicate whether mutations are present. A negative result can provide reassurance, while a positive result can guide further management and treatment options. It’s essential to discuss the findings with your healthcare provider for comprehensive understanding.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test | 468000 NGN | 520000 NGN |
How to Book the Test
To book the Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test, please contact us at +2348110567037 via call or WhatsApp. Our team is ready to assist you with the booking process and answer any questions you may have.
Additional Information
Turnaround Time: Sample Daily by 9 am; Report in 40 Working Days
Sample Type: Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. A duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Test Components: For MLPA negative cases*DMD
Pre-Test Instructions: A duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Specialty: Neurologist | Department: Molecular Diagnostics | Method: NGS, Sanger Sequencing | Disease Type: Genetic Disorders – Muscular Dystrophy