DNAJB2 Gene Spinal Muscular Atrophy Type 5 NGS Genetic DNA Test
Introduction
The DNAJB2 Gene Spinal Muscular Atrophy Type 5 NGS Genetic DNA Test is a cutting-edge diagnostic test that utilizes Next Generation Sequencing (NGS) technology to detect mutations in the DNAJB2 gene. This test is crucial for diagnosing spinal muscular atrophy type 5, a rare genetic disorder that affects motor neurons in the spinal cord, leading to muscle weakness and atrophy.
What the Test Measures
This genetic test specifically measures mutations in the DNAJB2 gene, which are associated with spinal muscular atrophy type 5. By identifying these mutations, healthcare providers can better understand the patient’s condition and tailor treatment plans accordingly.
Who Should Consider This Test
Individuals who exhibit symptoms of muscle weakness, reduced motor function, or have a family history of spinal muscular atrophy should consider this test. Risk factors include:
- Family history of genetic disorders
- Symptoms of muscle weakness or atrophy
- Neurological disorders
Benefits of Taking the Test
Taking the DNAJB2 Gene Spinal Muscular Atrophy Type 5 NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of spinal muscular atrophy type 5
- Informed decision-making for treatment and management
- Identification of at-risk family members
- Access to genetic counseling and support
Understanding Your Results
Once the test is completed, results will be provided to you and your healthcare provider. It is essential to discuss these results with a qualified genetic counselor or neurologist to understand their implications fully. They will help you interpret the findings and recommend any necessary follow-up actions.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| DNAJB2 Gene Spinal Muscular Atrophy Type 5 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the DNAJB2 Gene Spinal Muscular Atrophy Type 5 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient going for the test, along with a genetic counseling session to draw a pedigree chart of affected family members.
