POMT2 Gene Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Type C2 NGS Genetic DNA Test
Introduction
The POMT2 Gene Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Type C2 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect mutations in the POMT2 gene, which are associated with limb-girdle muscular dystrophy. This test employs Next-Generation Sequencing (NGS) technology, providing accurate and comprehensive results that can significantly impact patient care.
What the Test Measures
This genetic test analyzes the POMT2 gene for mutations that can lead to muscular dystrophy and dystroglycanopathy. By identifying these mutations, healthcare providers can better understand the underlying causes of muscle weakness and other related symptoms.
Who Should Consider This Test?
Individuals experiencing symptoms such as muscle weakness, difficulty with mobility, or family history of muscular dystrophy should consider this test. Risk factors include:
- Family history of limb-girdle muscular dystrophy
- Progressive muscle weakness
- Symptoms of dystroglycanopathy
Benefits of Taking the Test
Taking the POMT2 Gene test offers numerous benefits:
- Accurate diagnosis of genetic muscular disorders
- Guidance for treatment options
- Informed family planning and genetic counseling
- Understanding the risk of passing the condition to future generations
Understanding Your Results
Results from the POMT2 Gene test will indicate whether any mutations are present. A genetic counselor will help interpret these results, providing insights into their implications for health and family.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| POMT2 Gene Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Type C2 NGS Genetic DNA Test | 400,000 | 560,000 |
How to Book the Test
To book the POMT2 Gene Muscular Dystrophy-Dystroglycanopathy Limb-Girdle Type C2 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and providing any additional information you may need.
Pre-Test Instructions
Prior to taking the test, it is essential to gather a clinical history and consult with a genetic counselor. This session will help draw a pedigree chart of family members affected by the POMT2 gene disorder, ensuring a comprehensive understanding of the genetic background.
At DNA Labs Nigeria, we are committed to providing you with the highest quality diagnostic services. Take the first step towards understanding your health today!
