Sickle Cell Anemia Trio Prenatal Mutation Detection Test
Introduction
The Sickle Cell Anemia Trio Prenatal Mutation Detection Test is a vital diagnostic tool designed for expectant parents who are at risk of having a child with sickle cell anemia. This test identifies specific mutations in the HBB gene, which are responsible for the disorder. Understanding these genetic factors can significantly impact family planning and the health of the baby.
What the Test Measures
This test measures and detects mutations in the HBB gene, which is critical for the production of hemoglobin. Sickle cell anemia occurs when there are mutations in this gene, leading to the production of abnormal hemoglobin, which can cause various health complications.
Who Should Consider This Test
Expecting parents who are carriers of the sickle cell trait or have a family history of sickle cell anemia should consider this test. Symptoms and risk factors include:
- Family history of sickle cell disease
- Known carrier status of either parent
- Ethnic backgrounds with higher prevalence (e.g., African, Mediterranean)
Benefits of Taking the Test
The Sickle Cell Anemia Trio Prenatal Mutation Detection Test offers several benefits:
- Early detection of potential genetic disorders in the fetus
- Informed decision-making for parents regarding pregnancy and future health management
- Peace of mind through knowledge of the baby’s health status
Understanding Your Results
Results from the test will indicate whether the fetus has inherited any mutations associated with sickle cell anemia. A genetic counselor or healthcare provider will help interpret these results and discuss the implications for the family.
Test Details
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Sickle Cell Anemia Trio Prenatal Mutation Detection Test | 260000 NGN | 360000 NGN |
Pre-Test Instructions
To ensure accurate results, a duly filled Prenatal Genetic Testing Consent Form (Form 18) and the Genomics Clinical Information Requisition Form (Form 20) are mandatory. Additionally, samples should include:
- 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube from both parents
- 10 mL (5 mL min.) Amniotic fluid in a sterile screw-capped container
Samples must be shipped refrigerated and should not be frozen.
Turnaround Time
Samples must be submitted by Monday at 11 AM, with reports available by Friday.
Contact Us to Book the Test
For more information or to book the Sickle Cell Anemia Trio Prenatal Mutation Detection Test, please call or WhatsApp us at +2348077798758. Ensure your baby’s health today!
