Nx Gen Sequencing Optic Atrophy Test
Introduction
The Nx Gen Sequencing Optic Atrophy Test is a vital diagnostic tool designed to identify genetic mutations associated with optic atrophy, a condition characterized by the degeneration of the optic nerve leading to vision loss. This test employs advanced Next Generation Sequencing (NGS) and Sanger sequencing methods to analyze specific genes that play a crucial role in optic nerve function. Understanding the genetic basis of optic atrophy can significantly impact patient management and treatment options.
What the Test Measures
This test measures and detects mutations in several key genes associated with optic atrophy, including:
- ACO2
- AFG3L2
- C12ORF65
- CISD2
- MFN2
- NR2F1
- OPA1
- OPA3
- SLC25A46
- SPG7
- TIMM8A
- TMEM126A
- WFS1
Who Should Consider This Test?
This test is recommended for individuals who are experiencing unexplained vision loss or have a family history of optic atrophy. Symptoms may include:
- Progressive loss of vision
- Difficulty in visual acuity
- Changes in color perception
Additionally, patients with risk factors such as a family history of genetic disorders affecting vision should consider this test.
Benefits of Taking the Test
- Identifies genetic mutations that may contribute to optic atrophy.
- Provides insights into potential treatment options and management strategies.
- Helps in understanding the hereditary nature of the condition.
- Facilitates informed decision-making for patients and their families.
Understanding Your Results
Results from the Nx Gen Sequencing Optic Atrophy Test will indicate the presence or absence of mutations in the analyzed genes. A genetic counselor or ophthalmologist will help interpret the results, providing guidance on the implications for treatment and management of the condition.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Nx Gen Sequencing Optic Atrophy Test | 573300 NGN | 637000 NGN |
Book Your Test Today!
To schedule your Nx Gen Sequencing Optic Atrophy Test, please call or WhatsApp us at +2348077798758. Ensure you complete the Whole Exome Sequencing Consent Form (Form 37) prior to your appointment. Sample collection is done daily by 9 am, and results will be available within 45 days.
