MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test
Introduction to the Test
The MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to assess genetic variations in the MSX2 gene, which is crucial for normal craniofacial development. This test employs Next-Generation Sequencing (NGS) technology to provide accurate and comprehensive insights into genetic disorders associated with dysmorphology.
What the Test Measures
This test specifically detects mutations or alterations in the MSX2 gene that can lead to conditions such as parietal foramina, which may affect cranial shape and structure. By analyzing the genetic code, clinicians can identify potential risks and implications for the patient’s health.
Who Should Consider This Test
Individuals who should consider the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test include:
- Those with a family history of dysmorphology or craniofacial abnormalities.
- Patients exhibiting symptoms related to cranial malformations.
- Individuals seeking genetic counseling for family planning.
Benefits of Taking the Test
The benefits of undergoing the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test include:
- Early identification of genetic conditions, allowing for timely intervention.
- Informed family planning decisions based on genetic risks.
- Access to targeted therapies and management strategies for affected individuals.
Understanding Your Results
Once the test is completed, you will receive a comprehensive report detailing any genetic alterations found. It is essential to discuss these results with a qualified healthcare provider to understand their implications fully. Genetic counseling sessions can also provide further insights and guidance based on your results.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the MSX2 Gene Parietal Foramina Type 1 NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you with scheduling your test and answering any questions you may have.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history of the patient is essential, along with a genetic counseling session to create a pedigree chart of family members affected by the MSX2 gene.
This test falls under the specialty of Pediatrics and the department of Genetics, focusing on dysmorphology through advanced NGS technology.
