CORIN Gene Preeclampsia/Eclampsia Type 5 NGS Genetic DNA Test
Introduction
The CORIN Gene Preeclampsia/Eclampsia Type 5 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to assess genetic predispositions to preeclampsia, a serious pregnancy complication. Utilizing Next-Generation Sequencing (NGS) technology, this test provides invaluable insights into a woman’s risk factors for developing preeclampsia, enabling healthcare providers to implement proactive measures to safeguard maternal and fetal health.
What the Test Measures
This genetic test specifically detects variants in the CORIN gene, which have been associated with an increased risk of developing preeclampsia. By analyzing DNA from a blood sample or extracted DNA, the test can reveal whether a woman carries genetic markers linked to this condition.
Who Should Consider This Test
Women who are pregnant or planning to conceive, especially those with a family history of preeclampsia or related conditions, should consider this test. Symptoms of preeclampsia can include high blood pressure, swelling, and protein in the urine. Risk factors include obesity, diabetes, and previous instances of preeclampsia.
Benefits of Taking the Test
- Early identification of genetic risks associated with preeclampsia.
- Informed decision-making regarding prenatal care and management.
- Potential for preventive measures to be taken before symptoms arise.
- Peace of mind for expectant mothers and their families.
Understanding Your Results
Results from the CORIN Gene Preeclampsia/Eclampsia Type 5 NGS Genetic DNA Test will indicate whether any genetic variants associated with preeclampsia are present. A genetic counseling session will be provided to help interpret the results and discuss potential implications for pregnancy management.
Test Details and Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| CORIN Gene Preeclampsia/Eclampsia Type 5 NGS Genetic DNA Test | 40,000 | 56,000 |
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. It is essential to provide a clinical history and undergo a genetic counseling session to chart affected family members.
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. Don’t wait to take charge of your health—call or WhatsApp us at +254711564616 to book your test today!
