SCN4A Gene Hyperkalemic Periodic Paralysis NGS Genetic DNA Test
Introduction
The SCN4A Gene Hyperkalemic Periodic Paralysis NGS Genetic DNA Test is a crucial diagnostic tool for individuals experiencing episodes of muscle weakness or paralysis. This test utilizes Next Generation Sequencing (NGS) technology to analyze the SCN4A gene, which plays a vital role in muscle function. Understanding your genetic makeup can provide insights into the management and treatment of this condition.
What the Test Measures
This test specifically detects mutations in the SCN4A gene that are associated with Hyperkalemic Periodic Paralysis, a condition characterized by episodes of muscle stiffness and weakness. By identifying these mutations, healthcare providers can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test
Individuals who experience:
- Recurrent muscle weakness or paralysis
- Family history of Hyperkalemic Periodic Paralysis
- Symptoms triggered by exercise, stress, or dietary changes
should consider undergoing this genetic test. Consulting with a neurologist or genetic counselor can provide further guidance on the need for testing.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions
- Personalized treatment plans based on genetic findings
- Informed family planning and risk assessment
- Access to specialized care and support
Understanding Your Results
Results from the SCN4A Gene Hyperkalemic Periodic Paralysis NGS Genetic DNA Test will indicate whether any mutations are present. A genetic counselor will help interpret the results, discuss their implications, and recommend further steps if necessary.
Test Pricing
| Discount Price | 40,000 KSh |
|---|---|
| Regular Price | 56,000 KSh |
Branches and Booking
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. To book the SCN4A Gene Hyperkalemic Periodic Paralysis NGS Genetic DNA Test, please contact us at +254711564616 or visit our website. Take the first step towards understanding your health today!
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood or extracted DNA, or even a drop of blood on an FTA card. Prior to the test, it is recommended to have a clinical history assessment and a genetic counseling session to create a pedigree chart of affected family members.
