CNGB3 Gene Achromatopsia Type 3 NGS Genetic DNA Test
Introduction
The CNGB3 Gene Achromatopsia Type 3 NGS Genetic DNA Test is an advanced diagnostic tool that helps identify mutations in the CNGB3 gene, responsible for achromatopsia. Achromatopsia is a genetic condition leading to color blindness and severe visual impairment. Understanding the genetic basis of this disorder is essential for effective management and support.
What the Test Measures
This test specifically detects mutations in the CNGB3 gene, which plays a critical role in the function of photoreceptors in the retina. By analyzing the DNA, the test can confirm or rule out achromatopsia type 3, providing valuable information for patients and their families.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Color blindness
- Light sensitivity
- Visual impairment
Additionally, those with a family history of achromatopsia or related conditions should consider this test. A genetic counseling session is recommended before testing to discuss potential outcomes and implications.
Benefits of Taking the Test
- Accurate diagnosis of achromatopsia type 3
- Informed family planning options
- Guidance for treatment and management strategies
- Access to support resources for affected individuals
Understanding Your Results
Results from the CNGB3 Gene Achromatopsia Type 3 NGS Genetic DNA Test will typically be available within 3 to 4 weeks. A genetic counselor will help interpret the results, discussing their implications for you and your family.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Branches and Booking
We have branches across all major cities in Kenya, offering convenient access to our services. For those unable to visit us in person, we also provide a home sample collection service.
To book the CNGB3 Gene Achromatopsia Type 3 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616. Take the first step towards understanding your genetic health today!
