FGFR2 Gene Craniosynostosis Nonspecific NGS Genetic DNA Test
The FGFR2 Gene Craniosynostosis Nonspecific NGS Genetic DNA Test is an advanced diagnostic test designed to identify genetic mutations that may lead to craniosynostosis. This condition involves the premature fusion of skull bones, which can affect head shape and potentially lead to increased intracranial pressure and developmental delays. Early detection through genetic testing can significantly improve management and outcomes for affected individuals.
What the Test Measures
This test specifically detects mutations in the FGFR2 gene, which is known to be associated with nonspecific craniosynostosis. By analyzing the DNA sample, healthcare providers can determine if a patient has inherited or developed mutations that contribute to this condition.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Children with abnormal head shapes or developmental delays.
- Families with a history of craniosynostosis or related syndromes.
- Patients exhibiting symptoms of increased intracranial pressure.
Benefits of Taking the Test
Taking the FGFR2 Gene Craniosynostosis Nonspecific NGS Genetic DNA Test offers several benefits:
- Early diagnosis of craniosynostosis, allowing for timely intervention.
- Informed clinical decisions regarding treatment options.
- Understanding family risk and implications for future pregnancies.
Understanding Your Results
Results from the FGFR2 Gene Craniosynostosis Nonspecific NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or medical professional. They will provide guidance on the implications of the results, including:
- Whether a mutation was detected.
- Possible health implications for the patient.
- Next steps for management or further testing.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To schedule the FGFR2 Gene Craniosynostosis Nonspecific NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and provide any additional information you may need.
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood or extracted DNA, or even one drop of blood on an FTA card. Prior to testing, a clinical history must be provided, and a genetic counseling session is recommended to create a pedigree chart of affected family members.
