RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test
Introduction
The RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test is a specialized diagnostic test designed to identify mutations in the RUNX2 gene, which are responsible for cleidocranial dysplasia (CCD). CCD is a genetic condition characterized by skeletal abnormalities, including underdeveloped or absent collarbones, dental issues, and other associated anomalies. This test is crucial for early diagnosis and management of the condition, allowing for informed medical decisions.
What the Test Measures
This genetic test specifically detects mutations in the RUNX2 gene, utilizing Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results. The analysis helps in confirming a diagnosis of cleidocranial dysplasia, enabling healthcare providers to tailor treatment plans accordingly.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Underdeveloped or absent collarbones
- Dental abnormalities
- Skeletal deformities
- Family history of cleidocranial dysplasia
are encouraged to consider this test. Additionally, those with a clinical history indicating potential genetic disorders should consult their healthcare provider for further evaluation.
Benefits of Taking the Test
Taking the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test offers several advantages:
- Accurate diagnosis of cleidocranial dysplasia.
- Informed decisions regarding treatment options.
- Identification of at-risk family members.
- Access to genetic counseling and support.
Understanding Your Results
Once the test is completed, results will be interpreted by a qualified geneticist or healthcare provider. It is important to understand that a positive result indicates the presence of a RUNX2 gene mutation, while a negative result suggests that no mutation was detected. However, further consultation may be necessary to fully understand the implications of the results.
Test Pricing
| Price Type | Price (KSh) |
|---|---|
| Discount Price | 40,000 KSh |
| Regular Price | 56,000 KSh |
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 RUNX2 gene.
Book Your Test Today!
We have branches across Kenya, making it easy for you to access the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test. For more information or to book your test, please call or WhatsApp us at +254711564616.
