Prenatal Alpha Thalassemia Mutation Screening 3 Common Mutation
Introduction
Prenatal Alpha Thalassemia Mutation Screening is a crucial diagnostic test that helps in identifying specific genetic mutations associated with alpha thalassemia, a blood disorder that can affect the health of an unborn child. This test is particularly important for expectant parents, as it provides early insights into potential genetic risks, allowing for better management and care during pregnancy.
What the Test Measures
This screening test detects three common mutations associated with alpha thalassemia. By analyzing the genetic material from the mother and the fetus, healthcare providers can determine the risk of the child inheriting thalassemia, which can lead to serious health complications if left undiagnosed.
Who Should Consider This Test
Expecting parents, particularly those with a family history of thalassemia or those belonging to high-risk ethnic groups, should consider this test. Symptoms indicating a potential risk include:
- Family history of blood disorders
- Ethnic background with higher prevalence of thalassemia
- Abnormal blood test results during pregnancy
Benefits of Taking the Test
- Early detection of potential genetic disorders
- Informed decision-making regarding pregnancy management
- Peace of mind for expecting parents
- Opportunity for early intervention if necessary
Understanding Your Results
Results from the Prenatal Alpha Thalassemia Mutation Screening will help you understand the genetic risks associated with alpha thalassemia. A healthcare provider will discuss the findings with you, explaining any necessary follow-up actions or tests that may be required based on the results.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Prenatal Alpha Thalassemia Mutation Screening | 150,000 NGN | 200,000 NGN |
Book the Test
To ensure a healthy pregnancy and gain valuable insights into your child’s health, book your Prenatal Alpha Thalassemia Mutation Screening today. For appointments, please call or WhatsApp us at +2348077798758. Don’t wait – secure your peace of mind now!
Additional Information
Turnaround Time: 10-12 days
Sample Type: Peripheral blood / Amniotic Fluid / Chorionic villi / Cord blood
Test Components: Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml)
Pre-Test Instructions: This screening can be done with a Doctor’s prescription. Note that a prescription is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.
Specialty
General Physician
