OAT Gene Gyrate Atrophy of Choroid and Retina With or Without Ornithinemia NGS Genetic DNA Test
Introduction
The OAT Gene Gyrate Atrophy of Choroid and Retina with or without Ornithinemia NGS Genetic DNA Test is a groundbreaking diagnostic tool designed to identify genetic mutations associated with serious ophthalmological disorders. This test employs Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results, crucial for patients and their families.
What the Test Measures
This genetic test detects mutations in the OAT gene, which are linked to gyrate atrophy of the choroid and retina, a condition that can lead to progressive vision loss. By analyzing the genetic material, the test provides insights into the presence or absence of these mutations.
Who Should Consider This Test?
Individuals experiencing symptoms such as:
- Progressive vision loss
- Night blindness
- Family history of retinal disorders
should consider this test. Additionally, those with risk factors like a clinical history of ornithinemia or related conditions are encouraged to seek testing.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders
- Informed decision-making regarding treatment options
- Guidance for family planning and genetic counseling
- Access to specialized care from geneticists and ophthalmologists
Understanding Your Results
Results from the OAT Gene Gyrate Atrophy test can help determine the presence of genetic mutations. A genetic counselor will assist in interpreting the results, providing clarity on what they mean for your health and potential impacts on family members.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| OAT Gene Gyrate Atrophy of Choroid and Retina With or Without Ornithinemia NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the OAT Gene Gyrate Atrophy of Choroid and Retina test today by calling or WhatsApping us at +2348077798758. Our team is ready to assist you in your journey towards better health.
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 by the OAT gene.
Consult with an ophthalmologist or geneticist to learn more about the implications of your results and the best steps forward.
