Nx Gen Sequencing Hereditary Retinoblastoma Test
Introduction to the Test
The Nx Gen Sequencing Hereditary Retinoblastoma Test is a state-of-the-art diagnostic tool that plays a crucial role in identifying genetic mutations linked to hereditary retinoblastoma, a rare but serious form of eye cancer. This test is designed for individuals who may be at risk due to family history, allowing for early detection and proactive management of the condition.
What the Test Measures
This test specifically measures mutations in the RB1 and MYCN genes, which are known to be associated with the development of retinoblastoma. By analyzing these genes, healthcare professionals can assess the risk of hereditary retinoblastoma in patients.
Who Should Consider This Test?
Individuals who should consider the Nx Gen Sequencing Hereditary Retinoblastoma Test include:
- Those with a family history of retinoblastoma or other eye cancers.
- Patients exhibiting symptoms such as abnormal eye movements, white pupils, or vision problems.
- Individuals with genetic predispositions to cancer.
Benefits of Taking the Test
- Early detection of hereditary retinoblastoma can lead to timely interventions, improving treatment outcomes.
- Understanding genetic risk factors helps in making informed decisions regarding surveillance and management.
- Access to specialized care from ophthalmologists and molecular diagnostics experts.
Understanding Your Results
Once the test is completed, results will be analyzed and communicated to you within 45 days. Your healthcare provider will help interpret the results, discussing any identified mutations and their implications for your health and that of your family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Nx Gen Sequencing Hereditary Retinoblastoma Test | 573300 NGN | 637000 NGN |
How to Book the Test
To schedule your Nx Gen Sequencing Hereditary Retinoblastoma Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and any inquiries you may have.
Important Pre-Test Instructions
Before taking the test, ensure you have a duly filled Whole Exome Sequencing Consent Form (Form 37) as it is mandatory for the testing process. Sample requirements include:
- Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes.
- Ship refrigerated. DO NOT FREEZE.
Test Components and Methodology
This test utilizes Next Generation Sequencing (NGS) and Sanger sequencing methods to provide accurate and reliable results, ensuring that patients receive the best possible care from our molecular diagnostics department.
Contact Us
For more information or to book your test, please reach out to us at +2348077798758. Your health is our priority!
