FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test
Introduction to the FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test
The FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test is a specialized genetic test that analyzes the FGFR2 gene for mutations that can lead to Crouzon syndrome, a genetic disorder characterized by the premature fusion of skull bones. This condition can result in various physical abnormalities, including facial deformities and neurological issues. Early detection through this test is crucial for timely management and intervention.
What the Test Measures
This test specifically measures mutations in the FGFR2 gene, which is known to be associated with Crouzon syndrome. By identifying these mutations, healthcare providers can better understand the genetic basis of the condition in affected individuals.
Who Should Consider This Test
This test is recommended for:
- Individuals with a family history of Crouzon syndrome.
- Patients displaying symptoms such as craniosynostosis, facial deformities, or other dysmorphologies.
- Parents who are concerned about the genetic risks for their children.
Benefits of Taking the Test
Undergoing the FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test provides several benefits, including:
- Early diagnosis and intervention, which can significantly improve patient outcomes.
- Informed family planning for individuals with a family history of the condition.
- Access to specialized care and management strategies tailored to the individual’s needs.
Understanding Your Results
Results from the FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test will be provided along with a detailed interpretation. It is essential to discuss these results with a healthcare provider or genetic counselor to understand their implications fully.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
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 even one drop of blood on an FTA card. Prior to the test, a clinical history of the patient is necessary, along with a genetic counseling session to draw a pedigree chart of family members affected by the FGFR2 gene.
Book Your Test Today!
We have branches across all major cities in Kenya, making it easy for you to access our services. For more information or to book the FGFR2 Gene Crouzon Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
