Thalassemia Beta Trio Prenatal Mutation Detection Test
Introduction
The Thalassemia Beta Trio Prenatal Mutation Detection Test is an essential diagnostic tool for expectant parents, particularly those with a family history of thalassemia or other genetic disorders. This test plays a pivotal role in identifying potential genetic mutations that could affect the health of the unborn child. Early detection allows for informed decision-making and management of the pregnancy, ensuring better outcomes for both mother and baby.
What the Test Measures
This test detects over 100 mutations associated with beta thalassemia, a genetic disorder that affects hemoglobin production in red blood cells. By analyzing the DNA from both parents and the amniotic fluid, healthcare providers can assess the risk of the child inheriting thalassemia.
Who Should Consider This Test
Expectant parents should consider the Thalassemia Beta Trio Prenatal Mutation Detection Test if:
- They have a family history of thalassemia or related genetic disorders.
- They are carriers of thalassemia mutations.
- They belong to ethnic groups with a higher prevalence of thalassemia, such as Mediterranean, Middle Eastern, or Southeast Asian descent.
- They are experiencing symptoms associated with thalassemia, such as anemia or fatigue.
Benefits of Taking the Test
Taking the Thalassemia Beta Trio Prenatal Mutation Detection Test offers numerous benefits, including:
- Early identification of genetic risks, allowing for informed prenatal care decisions.
- Peace of mind for parents regarding their baby’s health.
- Access to specialized care and management options if necessary.
- Empowerment through knowledge about potential genetic disorders.
Understanding Your Results
Results from the Thalassemia Beta Trio Prenatal Mutation Detection Test will indicate whether any mutations are present. A genetic counselor will help interpret the results, explaining their implications for the pregnancy and potential next steps. Understanding these results is crucial for making informed decisions regarding the health and management of the unborn child.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Thalassemia Beta Trio Prenatal Mutation Detection Test | 421200 NGN | 468000 NGN |
Booking the Test
To schedule the Thalassemia Beta Trio Prenatal Mutation Detection Test, please contact us at +2348077798758 or visit our website to book your appointment. Ensure you have the requisite forms filled out prior to testing for a seamless experience.
Test Details
Turnaround Time: Sample must be submitted by Monday 11 am; reports available by Friday.
Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube from both parents AND 10 mL (5 mL min.) amniotic fluid in a sterile screw-capped container. Ship refrigerated. DO NOT FREEZE.
Pre-Test Instructions: Duly filled Prenatal Genetic Testing Consent Form (Form 18) & Genomics Clinical Information Requisition Form (Form 20) is mandatory.
