CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 NGS Genetic DNA Test
Introduction
The CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 NGS Genetic DNA Test is a vital diagnostic tool for individuals suspected of having hypokalemic periodic paralysis, a rare neurological disorder. This test employs Next-Generation Sequencing (NGS) technology to analyze the CACNA1S gene, which plays a crucial role in muscle function and electrical signaling in the body.
What the Test Measures
This genetic test detects mutations in the CACNA1S gene that are associated with hypokalemic periodic paralysis. These mutations can lead to episodes of muscle weakness or paralysis, often triggered by factors such as stress, exercise, or low potassium levels.
Who Should Consider This Test
Individuals who experience:
- Recurrent episodes of muscle weakness or paralysis
- Family history of hypokalemic periodic paralysis
- Symptoms that worsen with exercise or stress
- Low potassium levels during episodes
should consider undergoing this test to confirm a diagnosis and guide treatment options.
Benefits of Taking the Test
- Accurate diagnosis of hypokalemic periodic paralysis
- Informed decision-making regarding treatment and management
- Identification of at-risk family members through genetic counseling
- Enhanced understanding of the condition and its implications
Understanding Your Results
Results from the CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 NGS Genetic DNA Test will indicate whether a mutation is present. A positive result confirms the diagnosis, while a negative result may suggest that another underlying cause is responsible for the symptoms. It is essential to discuss your results with a healthcare professional for proper interpretation and guidance.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Book Your Test Today!
We have branches across Kenya and offer a convenient home sample collection service. To book the CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Take the first step towards understanding your health today!
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
Pre-test instructions include a clinical history review and a genetic counseling session to draw a pedigree chart of family members affected with CACNA1S Gene Hypokalemic Periodic Paralysis Type 1.
Consult with a neurologist or genetic specialist to learn more about this test and its implications for your health.
