C21orf2 Gene Cone-Rod Dystrophy C21orf2 Related NGS Genetic DNA Test
Introduction to the Test
The C21orf2 Gene Cone-Rod Dystrophy C21orf2 Related NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with cone-rod dystrophy, a progressive eye disorder that can lead to vision loss. This test utilizes Next Generation Sequencing (NGS) technology to analyze the C21orf2 gene, which plays a critical role in the functioning of retinal cells.
What the Test Measures
This genetic test measures the integrity of the C21orf2 gene, detecting any mutations that may be responsible for cone-rod dystrophy. By examining the genetic material, healthcare providers can gain insights into the likelihood of developing this condition.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Progressive vision loss
- Difficulty seeing in low light
- Color vision deficiencies
Additionally, those with a family history of cone-rod dystrophy or related genetic disorders should consider this test to understand their genetic risk.
Benefits of Taking the Test
- Early diagnosis allows for timely intervention and management of symptoms.
- Informed family planning through genetic counseling.
- Access to clinical trials or new therapies targeting genetic disorders.
- Personalized treatment plans based on genetic findings.
Understanding Your Results
Results from the C21orf2 Gene Cone-Rod Dystrophy NGS Genetic DNA Test will provide essential information about the presence of mutations. A genetic counselor will help interpret the results, discussing their implications for you and your family.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| C21orf2 Gene Cone-Rod Dystrophy NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book your C21orf2 Gene Cone-Rod Dystrophy NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to schedule an appointment. Our team is here to assist you through every step of the testing 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. A genetic counseling session to draw a pedigree chart of family members affected with C21orf2 Gene Cone-Rod Dystrophy is recommended.
Consult with an ophthalmologist or a genetics specialist for more information regarding your eligibility for this test and its implications.
