Nx Gen Sequencing Ophthalmoplegia Test
Introduction
The Nx Gen Sequencing Ophthalmoplegia Test is a cutting-edge diagnostic tool designed to provide insights into the genetic factors contributing to ophthalmoplegia, a condition characterized by weakness or paralysis of the eye muscles. This test utilizes advanced next-generation sequencing (NGS) and Sanger sequencing methods to analyze specific genes associated with this condition, allowing healthcare providers to make informed decisions regarding patient care.
What the Test Measures
This test detects mutations in several key genes, including:
- C10orf2
- DNA2
- OPA1
- POLG
- POLG2
- RRM2B
- SLC25A4
- TYMP
By identifying these genetic variations, the Nx Gen Sequencing Ophthalmoplegia Test helps in understanding the underlying causes of eye muscle weakness.
Who Should Consider This Test?
This test is recommended for individuals who exhibit symptoms of ophthalmoplegia, including:
- Difficulty moving the eyes
- Drooping eyelids
- Double vision
- Eye muscle weakness
Additionally, those with a family history of genetic eye disorders or unexplained visual disturbances should consider this test as part of their diagnostic process.
Benefits of Taking the Test
- Accurate diagnosis of genetic causes of ophthalmoplegia.
- Guidance for treatment and management options.
- Informed family planning for individuals with hereditary conditions.
- Access to specialized care from ophthalmologists and genetic counselors.
Understanding Your Results
Results from the Nx Gen Sequencing Ophthalmoplegia Test will provide detailed information about any identified mutations. It is crucial to discuss these results with a healthcare provider who can explain their implications and recommend appropriate next steps.
Test Name and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Nx Gen Sequencing Ophthalmoplegia Test | 573300 NGN | 637000 NGN |
How to Book the Test
To book the Nx Gen Sequencing Ophthalmoplegia Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Pre-Test Instructions
For this test, it is mandatory to submit a duly filled Whole Exome Sequencing Consent Form (Form 37) along with your sample. Ensure that you provide a sample of 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes, shipped refrigerated and not frozen.
Turnaround Time
Samples should be submitted daily by 9 AM, with reports available in approximately 45 working days.
Trust DNA Labs Nigeria for your diagnostic needs. We are committed to providing accurate and timely results to help you manage your health effectively.
