CCM2 Gene Cerebral Cavernous Malformations Type 2 NGS Genetic DNA Test
Introduction
The CCM2 Gene Cerebral Cavernous Malformations Type 2 NGS Genetic DNA Test is a vital diagnostic tool designed to identify genetic mutations associated with cerebral cavernous malformations (CCMs). These vascular malformations can lead to serious neurological complications, including seizures and strokes. Understanding your genetic predisposition through this test can aid in early detection and management of potential health risks.
What the Test Measures
This genetic test employs Next-Generation Sequencing (NGS) technology to analyze the CCM2 gene for mutations that may contribute to the development of cerebral cavernous malformations. By identifying these genetic variations, healthcare providers can better understand the risk factors and potential health implications for the patient and their family.
Who Should Consider This Test?
Individuals who exhibit symptoms such as unexplained seizures, headaches, or neurological deficits may benefit from this test. Additionally, those with a family history of cerebral cavernous malformations or related vascular diseases should consider genetic testing to assess their risk and inform family planning decisions.
Benefits of Taking the Test
- Early diagnosis of potential health risks associated with CCM2 mutations.
- Informed decision-making for family planning and management of health.
- Access to targeted treatment options based on genetic findings.
- Improved understanding of the condition for patients and their families.
Understanding Your Results
Results from the CCM2 Gene test will provide insights into the presence of genetic mutations. It is essential to discuss these results with a healthcare provider to understand their implications fully. Genetic counseling may also be recommended to help interpret the results and discuss potential next steps.
Test Details and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| CCM2 Gene Cerebral Cavernous Malformations Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Information
To book the CCM2 Gene Cerebral Cavernous Malformations Type 2 NGS Genetic DNA Test, please contact us at +2348077798758 or reach out via WhatsApp. Our team is ready to assist you with any inquiries and guide you through the booking process.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected with the CCM2 gene.
Take control of your health today by understanding your genetic predisposition to cerebral cavernous malformations. Book your test now!
