Nx Gen Sequencing Familial Hemiplegic Migraine Test
Introduction to the Test
The Nx Gen Sequencing Familial Hemiplegic Migraine Test is a specialized genetic test that plays a crucial role in diagnosing familial hemiplegic migraine (FHM), a rare and debilitating form of migraine. Understanding the genetic basis of this condition can empower patients and their healthcare providers to make informed decisions regarding treatment and management.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) and Sanger sequencing methods to identify mutations in specific genes that are known to be associated with familial hemiplegic migraine. The key components of this test include:
- ATP1A2
- CACNA1A
- PRRT2
- SCN1A
Who Should Consider This Test?
This test is particularly beneficial for individuals who experience symptoms of familial hemiplegic migraine, which may include:
- Severe headache attacks accompanied by temporary paralysis
- Visual disturbances
- Neurological symptoms during migraine attacks
Additionally, those with a family history of migraine disorders may also consider testing to understand their risk factors better.
Benefits of Taking the Test
By undergoing the Nx Gen Sequencing Familial Hemiplegic Migraine Test, patients can:
- Gain insights into their genetic predisposition to migraines
- Make informed decisions regarding treatment and management
- Receive personalized care based on their genetic profile
- Understand family planning implications for hereditary conditions
Understanding Your Results
Results from the Nx Gen Sequencing Familial Hemiplegic Migraine Test will provide information about any detected genetic mutations. A qualified neurologist will interpret the results, explaining their significance and potential implications for your health and treatment options.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 46800 KSh | 52000 KSh |
Sample Collection and Instructions
To ensure accurate results, please submit 10 mL (5 mL minimum) of whole blood from 2 Lavender Top (EDTA) tubes, shipped refrigerated. It is crucial not to freeze the samples. A duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory before the test can be processed.
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. To book the Nx Gen Sequencing Familial Hemiplegic Migraine Test, please call or WhatsApp us at +254711564616.
