FGFR2 Gene Apert Syndrome NGS Genetic DNA Test
Introduction to the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test
The FGFR2 Gene Apert Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the FGFR2 gene. This gene is crucial in the development of various physical features and structures during embryonic growth. Identifying mutations in this gene is essential for diagnosing Apert syndrome, a genetic disorder characterized by craniosynostosis and limb abnormalities.
What the Test Measures
This test specifically detects alterations in the FGFR2 gene, which can lead to Apert syndrome and related dysmorphologies. By analyzing the genetic material, healthcare providers can determine the presence of specific mutations that may affect an individual’s health and development.
Who Should Consider This Test?
Individuals who may benefit from the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test include:
- Patients exhibiting symptoms of Apert syndrome, such as craniosynostosis or limb deformities.
- Individuals with a family history of genetic disorders, particularly those related to dysmorphology.
- Parents who have had children with congenital anomalies.
Benefits of Taking the Test
The benefits of the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test include:
- Early diagnosis of genetic disorders, allowing for timely intervention and management.
- Informed family planning for prospective parents.
- Access to specialized care and support tailored to genetic conditions.
- Peace of mind through understanding genetic risks and implications.
Understanding Your Results
Upon completion of the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test, results will be provided in a clear and understandable format. Healthcare professionals will assist in interpreting the results, discussing any identified mutations, and outlining potential implications for health and treatment options.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FGFR2 Gene Apert Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Convenient Testing Options
We have branches across all major cities in Kenya, providing easy access to the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test. Additionally, we offer a home sample collection service for your convenience.
Book Your Test Today!
Don’t wait to gain valuable insights into your genetic health. Call or WhatsApp us at +254711564616 to book the FGFR2 Gene Apert Syndrome NGS Genetic DNA Test today!
Turnaround time for results is approximately 3 to 4 weeks. Please ensure you have a clinical history prepared and consider a genetic counseling session to discuss family history related to FGFR2 gene mutations.
