Thalassemia Alpha Trio Prenatal Mutation Detection Test
Introduction
The Thalassemia Alpha Trio Prenatal Mutation Detection Test is an essential diagnostic tool designed for expectant parents to detect potential genetic mutations that could lead to thalassemia in their unborn child. This test plays a vital role in prenatal care, providing critical information that can influence medical decisions and prepare families for the future.
What the Test Measures
This test specifically measures mutations associated with thalassemia, a genetic blood disorder that affects hemoglobin production. By analyzing the genetic material from both parents and the amniotic fluid, the test can identify the presence of mutations that may lead to alpha thalassemia in the fetus.
Who Should Consider This Test
Expectant parents who have a family history of thalassemia or belong to populations with a higher prevalence of this genetic disorder should consider this test. Symptoms of thalassemia may not be apparent until later in life, making prenatal testing a proactive approach. Risk factors include:
- Family history of thalassemia or other genetic disorders
- Ethnic background associated with higher rates of thalassemia
- Previous pregnancies affected by genetic disorders
Benefits of Taking the Test
- Early detection of genetic disorders, allowing for informed decision-making.
- Peace of mind for parents regarding the health of their unborn child.
- Opportunity for early intervention and management of potential health issues.
Understanding Your Results
Results from the Thalassemia Alpha Trio Prenatal Mutation Detection Test will indicate whether any mutations were detected in the fetus. A healthcare professional will provide guidance on interpreting results and discussing potential implications for the pregnancy.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Thalassemia Alpha Trio Prenatal Mutation Detection Test | 320,000 NGN | 440,000 NGN |
Booking Information
To book the Thalassemia Alpha Trio Prenatal Mutation Detection Test, please ensure you have the following:
- 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
- Duly filled Prenatal Genetic Testing Consent Form (Form 18)
- Duly filled Genomics Clinical Information Requisition Form (Form 20)
Samples should be shipped refrigerated and must not be frozen. The turnaround time for results is typically one week, with samples submitted by Monday at 9 AM and reports available by Friday.
For more information or to book your test, please call or WhatsApp us at +2348077798758.
