Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test
Introduction to the Test
The Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test is a cutting-edge diagnostic test designed to detect genetic mutations associated with Duchenne and Becker muscular dystrophy (DMD/BMD). These conditions primarily affect muscle strength and function, leading to progressive muscle degeneration. Early diagnosis is crucial for effective management and treatment, making this test an essential tool in neurology and molecular diagnostics.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) and Sanger sequencing methods to identify mutations in the dystrophin gene, which is responsible for producing dystrophin, a protein crucial for muscle health. By analyzing the genetic code, the test can reveal the presence of mutations that may lead to DMD or BMD.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Children showing symptoms of muscle weakness or delayed motor skills.
- Family members of diagnosed patients, as DMD/BMD can be hereditary.
- Individuals with a family history of muscular dystrophy.
Symptoms such as difficulty in running, jumping, or climbing stairs may prompt consideration of this test.
Benefits of Taking the Test
Taking the Nx Gen Sequencing test offers numerous benefits:
- Early diagnosis can lead to timely interventions and treatment options.
- Understanding genetic risks can help in family planning and management.
- Provides clarity on the specific type of muscular dystrophy, aiding in personalized treatment strategies.
Understanding Your Results
Results from the Nx Gen Sequencing test will indicate whether mutations are present in the dystrophin gene. A positive result may confirm a diagnosis of DMD/BMD, while a negative result can provide reassurance. It is important to discuss results with a healthcare provider to understand their implications and next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test | 46,800 KSh | 52,000 KSh |
Sample Submission and Pre-Test Instructions
To conduct the test, submit 10 mL (5 mL min.) of whole blood from 2 Lavender Top (EDTA) tubes. It is essential that the sample is shipped refrigerated and not frozen. A duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory for processing.
Branches Across Kenya
We have branches in all major cities across Kenya, providing accessible testing services. Additionally, we offer a home sample collection service for your convenience.
Book Your Test Today!
Don’t wait for symptoms to progress. Book the Nx Gen Sequencing Duchenne Becker Muscular Dystrophy Test today by calling or WhatsApp messaging us at +254711564616.
