CCDC8 Gene Three M Syndrome Type 3 NGS Genetic DNA Test
Introduction
The CCDC8 Gene Three M Syndrome Type 3 NGS Genetic DNA Test is an advanced diagnostic tool that plays a pivotal role in identifying genetic mutations linked to Three M syndrome. This genetic condition can lead to significant health challenges, making early detection essential for effective management and intervention.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the CCDC8 gene, which is crucial in the development of various physical characteristics associated with Three M syndrome. By detecting mutations in this gene, healthcare providers can better understand the genetic underpinnings of the condition.
Who Should Consider This Test?
Individuals who exhibit symptoms of dysmorphology or have a family history of Three M syndrome should consider this test. Common symptoms may include:
- Distinctive facial features
- Growth abnormalities
- Developmental delays
If you or your family members have experienced these symptoms, it may be beneficial to undergo testing.
Benefits of Taking the Test
- Early detection of genetic disorders
- Informed decision-making regarding health management
- Peace of mind for patients and families
- Access to tailored healthcare strategies based on genetic insights
Understanding Your Results
Upon completion of the CCDC8 Gene Three M Syndrome Type 3 NGS Genetic DNA Test, results will be provided within 3 to 4 weeks. It is essential to discuss these results with a healthcare professional who can help interpret the findings and guide further action if necessary.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To ensure the best care and access to this essential genetic test, please contact us at DNA Labs Nigeria. You can call or WhatsApp us at +2348077798758 to book your appointment today!
Pre-Test Instructions
Before undergoing the CCDC8 Gene Three M Syndrome Type 3 NGS Genetic DNA Test, it is recommended to have a genetic counseling session. This session will help draw a pedigree chart of family members affected by the condition, providing valuable context for the testing process.
With the CCDC8 Gene Three M Syndrome Type 3 NGS Genetic DNA Test, you take a proactive step towards understanding your genetic health and ensuring the well-being of your family.
