Notch3 Mutation Detection CADASIL Test
Introduction to the Notch3 Mutation Detection CADASIL Test
The Notch3 Mutation Detection CADASIL Test is a vital diagnostic tool for identifying mutations in the NOTCH3 gene, which are associated with CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy). This genetic disorder affects the small blood vessels in the brain, leading to neurological issues such as migraines, strokes, and cognitive decline. Early detection through this test can significantly impact patient management and treatment strategies.
What the Test Measures
This test specifically detects mutations in the NOTCH3 gene, which are critical in diagnosing CADASIL. By analyzing a sample of your blood, we can determine the presence of these genetic mutations, enabling healthcare providers to make informed decisions regarding your health.
Who Should Consider This Test?
Individuals who exhibit symptoms such as recurrent migraines, unexplained strokes, or cognitive decline should consider the Notch3 Mutation Detection CADASIL Test. Additionally, those with a family history of CADASIL or related neurological disorders are at higher risk and may benefit from testing.
Benefits of Taking the Test
- Early diagnosis of CADASIL can lead to prompt management and treatment.
- Understanding your genetic risk allows for better family planning and awareness.
- Guidance for lifestyle changes and preventive measures can be provided based on test results.
- Access to specialized care from neurologists and genetic counselors.
Understanding Your Results
Upon receiving your test results, it is essential to consult with your healthcare provider to interpret the findings accurately. A positive result indicates the presence of a mutation in the NOTCH3 gene, confirming a diagnosis of CADASIL. Your provider will discuss the implications of the results and the next steps for managing your health.
Test Pricing
Test Name | Discount Price (NGN) | Regular Price (NGN) |
---|---|---|
Notch3 Mutation Detection CADASIL Test | 260,000 NGN | 360,000 NGN |
How to Book the Test
To schedule your Notch3 Mutation Detection CADASIL Test, please contact us at +2348077798758 or visit our website to book your appointment. Ensure you bring a duly filled Genomics Clinical Information Requisition Form (Form 20) when you come for your test.
Test Details
- Turnaround Time: Sample Mon by 11 am; Report Fri
- Sample Type: 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Test Components: NOTCH3 Gene
- Pre-test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
- Specialty: Neurologist
- Department: Molecular Diagnostics
- Method: PCR, Sequencing
- Disease Type: Neurologic Disorder