RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test
Introduction to the Test
The RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test is a specialized genetic test designed to diagnose cleidocranial dysplasia (CCD), a rare genetic disorder that affects bone and dental development. This condition is primarily caused by mutations in the RUNX2 gene, which plays a critical role in the formation of bones and teeth. Understanding the genetic basis of CCD is crucial for effective management and treatment of the condition.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the RUNX2 gene. By analyzing the genetic material, the test can detect specific changes that may lead to cleidocranial dysplasia. This allows for a definitive diagnosis, which is essential for appropriate medical care.
Who Should Consider This Test?
Individuals who may benefit from the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test include:
- Those exhibiting symptoms of cleidocranial dysplasia, such as delayed closure of fontanelles, skeletal abnormalities, and dental issues.
- Individuals with a family history of CCD, as the condition is inherited in an autosomal dominant manner.
- Patients with unexplained skeletal anomalies that may suggest a genetic disorder.
Benefits of Taking the Test
Taking the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test offers several benefits:
- Provides a definitive diagnosis for individuals suspected of having cleidocranial dysplasia.
- Facilitates early intervention and management strategies to address associated health issues.
- Helps in understanding the genetic risks for family members and future generations.
- Guides healthcare providers in tailoring treatment plans based on genetic findings.
Understanding Your Results
Once the test is completed, results will be provided within 3 to 4 weeks. It is essential to consult with a genetic counselor or a healthcare professional to interpret the results accurately. They will explain the implications of the findings, including potential risks for family members and recommendations for further management.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To book the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Pre-Test Instructions
Before undergoing the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test, patients should:
- Provide a detailed clinical history.
- Attend a genetic counseling session to create a pedigree chart of family members affected by cleidocranial dysplasia.
Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
