Microcephaly Gene Panel
Introduction to the Microcephaly Gene Panel
The Microcephaly Gene Panel is a specialized genetic test aimed at identifying genetic mutations that may contribute to microcephaly, a condition characterized by an abnormally small head and associated developmental issues. Understanding the genetic factors involved is vital for early diagnosis, management, and intervention strategies.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect genetic variations associated with microcephaly. By analyzing samples from amniotic fluid, chorionic villi, or peripheral blood, the Microcephaly Gene Panel provides insights into potential genetic abnormalities.
Who Should Consider This Test?
- Individuals with a family history of microcephaly or related genetic disorders.
- Pregnant women with abnormal ultrasound findings.
- Parents concerned about developmental delays in their children.
Benefits of Taking the Test
- Early identification of genetic disorders associated with microcephaly.
- Informed decision-making regarding pregnancy and family planning.
- Access to specialized care and interventions based on genetic findings.
Understanding Your Results
Results from the Microcephaly Gene Panel will indicate the presence or absence of specific genetic mutations. A genetic counselor or healthcare provider will help interpret these results, guiding you on the next steps based on the findings.
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Microcephaly Gene Panel | 720,000 NGN | 960,000 NGN |
Book the Test Today!
To schedule your Microcephaly Gene Panel test, please contact us at +2348077798758. Ensure you have a doctor’s prescription prior to the test, as it is required for the procedure. Please note that prescriptions are not applicable for surgery and pregnancy cases or individuals planning to travel abroad.
Turnaround time for results is approximately 4-6 weeks. We look forward to assisting you with your genetic health needs.
